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nsv5485476

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,025

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 27 studies. See in: genome view    
Submitted genomic128,748,870-128,749,894Question Mark
Overlapping variant regions from other studies: 121 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):128,388,924-128,389,948Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485476Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7128,748,870128,749,894
nsv5485476RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7128,388,924128,389,948

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17002585deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17002585Submitted genomicNC_000007.14:g.128
748870_128749894de
l
GRCh38 (hg38)NC_000007.14Chr7128,748,870128,749,894
nssv17002585RemappedPerfectNC_000007.13:g.128
388924_128389948de
l
GRCh37.p13First PassNC_000007.13Chr7128,388,924128,389,948

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)
nssv17002585<0.00116404
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