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nsv5407478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 28 studies. See in: genome view    
Submitted genomic121,331,506-121,331,557Question Mark
Overlapping variant regions from other studies: 113 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):120,971,560-120,971,611Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7121,331,506121,331,557
nsv5407478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7120,971,560120,971,611

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17005000alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17005000Submitted genomicNC_000007.14:g.121
331506_121331557in
s280
GRCh38 (hg38)NC_000007.14Chr7121,331,506121,331,557
nssv17005000RemappedPerfectNC_000007.13:g.120
971560_120971611in
s280
GRCh37.p13First PassNC_000007.13Chr7120,971,560120,971,611

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)
nssv170050000.003226404
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