A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34832



Internal ID12644182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2638872..3091456hg38UCSC Ensembl
Innerchr10:2681064..3133648hg19UCSC Ensembl
Innerchr10:2671064..3123648hg18UCSC Ensembl
Innerchr10:2671064..3123648hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38452585
hg19452585
hg18452585
hg17452585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6990486, essv6985997, essv6980473, essv6980474, essv6985998
SamplesNA19201
Known GenesPFKP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34832
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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