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nsv4531165

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:364,637

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 265 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):49,574,421-49,939,057Question Mark
Overlapping variant regions from other studies: 265 SVs from 18 studies. See in: genome view    
Submitted genomic47,100,791-47,465,427Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4531165RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1849,574,42149,939,057
nsv4531165Submitted genomicGRCh37.p13Primary AssemblyNC_000018.9Chr1847,100,79147,465,427

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15960693duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15960693RemappedPerfectNC_000018.10:g.495
74421_49939057dup
GRCh38.p12First PassNC_000018.10Chr1849,574,42149,939,057
nssv15960693Submitted genomicNC_000018.9:g.4710
0791_47465427dup
GRCh37.p13NC_000018.9Chr1847,100,79147,465,427

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)
nssv159606934.6e-005121692
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