A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703938



Internal ID15093904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32627860..32647462hg38UCSC Ensembl
Innerchr19:33118766..33138368hg19UCSC Ensembl
Innerchr19:37810606..37830208hg18UCSC Ensembl
Innerchr19:37810606..37830208hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3819603
hg1919603
hg1819603
hg1719603
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527490
Supporting Variants
Samples
Known GenesANKRD27
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703938
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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