A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751538



Internal ID12985090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85282336..85569198hg38UCSC Ensembl
Innerchr15:85825567..86112429hg19UCSC Ensembl
Innerchr15:83626571..83913433hg18UCSC Ensembl
Innerchr15:83626571..83913433hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38286863
hg19286863
hg18286863
hg17286863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6985318, essv6987217, essv6988920, essv6985319, essv6987216
SamplesSPC_141
Known GenesAKAP13
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)esv2751538
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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