A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703068



Internal ID15093034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17273458..17284194hg38UCSC Ensembl
Innerchr19:17384267..17395003hg19UCSC Ensembl
Innerchr19:17245267..17256003hg18UCSC Ensembl
Innerchr19:17245267..17256003hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3810737
hg1910737
hg1810737
hg1710737
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515965
Supporting Variants
Samples
Known GenesANKLE1, BABAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703068
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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