A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35063



Internal ID12991099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57812923..58012428hg38UCSC Ensembl
Innerchr10:59572683..59772188hg19UCSC Ensembl
Innerchr10:59242689..59442194hg18UCSC Ensembl
Innerchr10:59242689..59442194hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38199506
hg19199506
hg18199506
hg17199506
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6979563, essv6979565, essv6988199, essv6979564, essv6979562
SamplesNA18572
Known Genes
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)esv35063
Frequency
Sample Size771
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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