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nsv3219808

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,600

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 20 studies. See in: genome view    
Submitted genomic40,089,101-40,092,700Question Mark
Overlapping variant regions from other studies: 123 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):38,245,354-38,248,953Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3219808Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1740,089,10140,092,700
nsv3219808RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1738,245,35438,248,953

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14431998deletionHG00514Optical mapping, SequencingOptical mapping, Sequence alignment, de novo and local sequence assembly39,861

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14431998Submitted genomicNC_000017.11:g.400
89101_40092700del3
599
GRCh38 (hg38)NC_000017.11Chr1740,089,10140,092,700
nssv14431998RemappedPerfectNC_000017.10:g.382
45354_38248953del3
599
GRCh37.p13First PassNC_000017.10Chr1738,245,35438,248,953

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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