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nsv4711439

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 174 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):110,948,966-110,948,966Question Mark
Overlapping variant regions from other studies: 115 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):136,275,843-136,275,843Question Mark
Overlapping variant regions from other studies: 175 SVs from 27 studies. See in: genome view    
Submitted genomic110,284,665-110,284,665Question Mark
Overlapping variant regions from other studies: 115 SVs from 22 studies. See in: genome view    
Submitted genomic136,596,981-136,596,981Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv4711439RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5110,948,966110,948,966+
nsv4711439RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6136,275,843136,275,843+
nsv4711439Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000005.9Chr5110,284,665110,284,665+
nsv4711439Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6136,596,981136,596,981+

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv16248116interchromosomal translocationB381SequencingPaired-end mapping15,743

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv16248116RemappedPerfectGRCh38.p12First PassNC_000005.10Chr5110,948,966110,948,966+
nssv16248116RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6136,275,843136,275,843+
nssv16248116Submitted genomicGRCh37 (hg19)NC_000005.9Chr5110,284,665110,284,665+
nssv16248116Submitted genomicGRCh37 (hg19)NC_000006.11Chr6136,596,981136,596,981+

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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