A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703777



Internal ID15440429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1684138..1695177hg38UCSC Ensembl
Innerchr19:1684137..1695176hg19UCSC Ensembl
Innerchr19:1635137..1646176hg18UCSC Ensembl
Innerchr19:1635137..1646176hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811040
hg1911040
hg1811040
hg1711040
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527350
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703777
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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