U.S. flag

An official website of the United States government

nsv2781959

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 284 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):7,846,337-7,846,337Question Mark
Overlapping variant regions from other studies: 284 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):7,846,342-7,846,342Question Mark
Overlapping variant regions from other studies: 211 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):82,285,382-82,285,382Question Mark
Overlapping variant regions from other studies: 211 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):82,285,384-82,285,384Question Mark
Overlapping variant regions from other studies: 284 SVs from 24 studies. See in: genome view    
Submitted genomic7,846,450-7,846,450Question Mark
Overlapping variant regions from other studies: 284 SVs from 24 studies. See in: genome view    
Submitted genomic7,846,455-7,846,455Question Mark
Overlapping variant regions from other studies: 211 SVs from 33 studies. See in: genome view    
Submitted genomic80,243,258-80,243,258Question Mark
Overlapping variant regions from other studies: 211 SVs from 33 studies. See in: genome view    
Submitted genomic80,243,260-80,243,260Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv2781959RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr57,846,3377,846,337-
nsv2781959RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr57,846,3427,846,342+
nsv2781959RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1782,285,38282,285,382+
nsv2781959RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1782,285,38482,285,384-
nsv2781959Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr57,846,4507,846,450-
nsv2781959Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr57,846,4557,846,455+
nsv2781959Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1780,243,25880,243,258+
nsv2781959Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1780,243,26080,243,260-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisClinVar IDOther Calls in this Sample and Study
nssv13660463interchromosomal translocationNIJ3SequencingSplit read and paired-end mappingSCV000320955nssv13660462
nssv13660462interchromosomal translocationNIJ3SequencingSplit read and paired-end mappingSCV000320955nssv13660463

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv13660463RemappedPerfectGRCh38.p12First PassNC_000005.10Chr57,846,3377,846,337-
nssv13660462RemappedPerfectGRCh38.p12First PassNC_000005.10Chr57,846,3427,846,342+
nssv13660463RemappedPerfectGRCh38.p12First PassNC_000017.11Chr1782,285,38282,285,382+
nssv13660462RemappedPerfectGRCh38.p12First PassNC_000017.11Chr1782,285,38482,285,384-
nssv13660463Submitted genomicGRCh37 (hg19)NC_000005.9Chr57,846,4507,846,450-
nssv13660462Submitted genomicGRCh37 (hg19)NC_000005.9Chr57,846,4557,846,455+
nssv13660463Submitted genomicGRCh37 (hg19)NC_000017.10Chr1780,243,25880,243,258+
nssv13660462Submitted genomicGRCh37 (hg19)NC_000017.10Chr1780,243,26080,243,260-

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDSample IDTypeClinical InterpretationClinVar IDGenderOther Calls in this Sample and Study
nssv13660463NIJ3interchromosomal translocationSCV000320955Femalenssv13660462
nssv13660462NIJ3interchromosomal translocationSCV000320955Femalenssv13660463

No genotype data were submitted for this variant

You are here: NCBI
Support Center