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nsv5477197

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:901

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 19 studies. See in: genome view    
Submitted genomic45,010,721-45,011,621Question Mark
Overlapping variant regions from other studies: 84 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):45,050,320-45,051,220Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5477197Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr745,010,72145,011,621
nsv5477197RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr745,050,32045,051,220

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16997350deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16997350Submitted genomicNC_000007.14:g.450
10721_45011621del
GRCh38 (hg38)NC_000007.14Chr745,010,72145,011,621
nssv16997350RemappedPerfectNC_000007.13:g.450
50320_45051220del
GRCh37.p13First PassNC_000007.13Chr745,050,32045,051,220

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)
nssv16997350<0.00126404
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