A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751782



Internal ID12638648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20638696..20802654hg38UCSC Ensembl
Innerchr19:20821502..20985460hg19UCSC Ensembl
Innerchr19:20613342..20777300hg18UCSC Ensembl
Innerchr19:20613342..20777300hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38163959
hg19163959
hg18163959
hg17163959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6983784, essv6987415
SamplesBEC_626
Known GenesZNF626
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751782
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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