A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34318



Internal ID12643671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82614804..82784743hg38UCSC Ensembl
Innerchr15:83283555..83453495hg19UCSC Ensembl
Innerchr15:81080610..81250549hg18UCSC Ensembl
Innerchr15:81080610..81250549hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38169940
hg19169941
hg18169940
hg17169940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6979095, essv6988101, essv6989066
SamplesNA12891
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
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)esv34318
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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