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nsv5491528

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:293

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 24 studies. See in: genome view    
Submitted genomic137,973,130-137,973,422Question Mark
Overlapping variant regions from other studies: 104 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):137,657,876-137,658,168Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5491528Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7137,973,130137,973,422
nsv5491528RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7137,657,876137,658,168

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17003711deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17003711Submitted genomicNC_000007.14:g.137
973130_137973422de
l
GRCh38 (hg38)NC_000007.14Chr7137,973,130137,973,422
nssv17003711RemappedPerfectNC_000007.13:g.137
657876_137658168de
l
GRCh37.p13First PassNC_000007.13Chr7137,657,876137,658,168

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)
nssv17003711<0.00146404
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