A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35106



Internal ID12991142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82629847..82677464hg38UCSC Ensembl
Innerchr10:84389603..84437220hg19UCSC Ensembl
Innerchr10:84379583..84427200hg18UCSC Ensembl
Innerchr10:84379583..84427200hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3847618
hg1947618
hg1847618
hg1747618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6979296, essv6979295, essv6979297
SamplesNA18524
Known GenesNRG3
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)esv35106
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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