A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988920



Internal ID12983132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85287462..85561683hg38UCSC Ensembl
Innerchr15:85830693..86104914hg19UCSC Ensembl
Innerchr15:83631697..83905918hg18UCSC Ensembl
Innerchr15:83631697..83905918hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38274222
hg19274222
hg18274222
hg17274222
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751538
Supporting Variants
SamplesSPC_141
Known GenesAKAP13
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988920
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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