A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751543



Internal ID12985095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93610267..93742908hg38UCSC Ensembl
Innerchr15:94153496..94286137hg19UCSC Ensembl
Innerchr15:91954500..92087141hg18UCSC Ensembl
Innerchr15:91954500..92087141hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38132642
hg19132642
hg18132642
hg17132642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6989525, essv6981837, essv6981836, essv6989265
SamplesBEC_492
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)esv2751543
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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