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nsv4125611

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 56 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):141,215,428-141,236,428Question Mark
Overlapping variant regions from other studies: 54 SVs from 7 studies. See in: genome view    
Submitted genomic140,595,000-140,616,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4125611RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5141,215,428141,236,428
nsv4125611Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr5140,595,000140,616,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15904835deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15904835RemappedPerfectNC_000005.10:g.141
215428_141236428de
l
GRCh38.p12First PassNC_000005.10Chr5141,215,428141,236,428
nssv15904835Submitted genomicNC_000005.9:g.1405
95000_140616000del
GRCh37.p13NC_000005.9Chr5140,595,000140,616,000

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)
nssv15904835<0.001321430
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