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nsv4877418

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:357,213

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1823 SVs from 90 studies. See in: genome view    
Remapped(Score: Perfect):68,028,115-68,385,327Question Mark
Overlapping variant regions from other studies: 1823 SVs from 90 studies. See in: genome view    
Submitted genomic65,695,352-66,052,564Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4877418RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000018.10Chr1868,028,11568,385,327
nsv4877418Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000018.9Chr1865,695,35266,052,564

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16410073inversionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16410073RemappedPerfectNC_000018.10:g.680
28115_68385327inv
GRCh38.p12First PassNC_000018.10Chr1868,028,11568,385,327
nssv16410073Submitted genomicNC_000018.9:g.6569
5352_66052564inv
GRCh37 (hg19)NC_000018.9Chr1865,695,35266,052,564

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16410073<0.001116834
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