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nsv4269113

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:292

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 18 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):42,950,939-42,951,230Question Mark
Overlapping variant regions from other studies: 16 SVs from 6 studies. See in: genome view    
Submitted genomic41,102,956-41,103,247Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4269113RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1742,950,93942,951,230
nsv4269113Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1741,102,95641,103,247

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15833198deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15833198RemappedPerfectNC_000017.11:g.429
50939_42951230del
GRCh38.p12First PassNC_000017.11Chr1742,950,93942,951,230
nssv15833198Submitted genomicNC_000017.10:g.411
02956_41103247del
GRCh37.p13NC_000017.10Chr1741,102,95641,103,247

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv158331984.6e-005121694
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