A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751533



Internal ID12638399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34484566..34692790hg38UCSC Ensembl
Innerchr15:34776767..34984991hg19UCSC Ensembl
Innerchr15:32564059..32772283hg18UCSC Ensembl
Innerchr15:32564059..32772283hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38208225
hg19208225
hg18208225
hg17208225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6989873, essv6983884
SamplesBEC_728
Known GenesGOLGA8B, MIR1233-1, MIR1233-2, MIR5588
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)esv2751533
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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