A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751539



Internal ID12985091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87219818..87326577hg38UCSC Ensembl
Innerchr15:87763049..87869808hg19UCSC Ensembl
Innerchr15:85564053..85670812hg18UCSC Ensembl
Innerchr15:85564053..85670812hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38106760
hg19106760
hg18106760
hg17106760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv111e55
Supporting Variantsessv6982181, essv6982180
SamplesBEC_400
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)esv2751539
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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