A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679642



Internal ID15416294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15979115..15990108hg38UCSC Ensembl
Innerchr19:16089925..16100918hg19UCSC Ensembl
Innerchr19:15950925..15961918hg18UCSC Ensembl
Innerchr19:15950925..15961918hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3810994
hg1910994
hg1810994
hg1710994
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520592
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679642
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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