A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672591



Internal ID15062557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6750193..6760963hg38UCSC Ensembl
Innerchr19:6750204..6760974hg19UCSC Ensembl
Innerchr19:6701204..6711974hg18UCSC Ensembl
Innerchr19:6701204..6711974hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810771
hg1910771
hg1810771
hg1710771
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519561
Supporting Variants
Samples
Known GenesSH2D3A, TRIP10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672591
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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