U.S. flag

An official website of the United States government

nsv4206200

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:295

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 11 SVs from 3 studies. See in: genome view    
Remapped(Score: Perfect):77,100,911-77,101,205Question Mark
Overlapping variant regions from other studies: 11 SVs from 3 studies. See in: genome view    
Submitted genomic76,811,957-76,812,251Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4206200RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1177,100,91177,101,205
nsv4206200Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1176,811,95776,812,251

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15953605duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15953605RemappedPerfectNC_000011.10:g.771
00911_77101205dup
GRCh38.p12First PassNC_000011.10Chr1177,100,91177,101,205
nssv15953605Submitted genomicNC_000011.9:g.7681
1957_76812251dup
GRCh37.p13NC_000011.9Chr1176,811,95776,812,251

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)
nssv159536054.6e-005121694
Support Center