A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751530



Internal ID12638396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31604809..32219354hg38UCSC Ensembl
Innerchr15:31897012..32511555hg19UCSC Ensembl
Innerchr15:29684304..30298847hg18UCSC Ensembl
Innerchr15:29684304..30298847hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38614546
hg19614544
hg18614544
hg17614544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109e55
Supporting Variantsessv6981829, essv6981828, essv6985673, essv6981827
SamplesBEC_491
Known GenesCHRNA7, OTUD7A
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)esv2751530
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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