A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751981



Internal ID12985533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162145671..162298510hg38UCSC Ensembl
Innerchr3:161863459..162016298hg19UCSC Ensembl
Innerchr3:163346153..163498992hg18UCSC Ensembl
Innerchr3:163346161..163499000hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38152840
hg19152840
hg18152840
hg17152840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6987684, essv6988849, essv6984796
SamplesSPC_18
Known Genes
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)esv2751981
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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