A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34828



Internal ID12990864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41364837..41466005hg38UCSC Ensembl
Innerchr3:41406328..41507496hg19UCSC Ensembl
Innerchr3:41381332..41482500hg18UCSC Ensembl
Innerchr3:41381332..41482500hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38101169
hg19101169
hg18101169
hg17101169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6980059, essv6980058, essv6988305, essv6980060
SamplesNA18947
Known GenesULK4
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)esv34828
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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