A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980892



Internal ID12635548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99817772..100051772hg38UCSC Ensembl
Innerchr15:100357977..100591977hg19UCSC Ensembl
Innerchr15:98175500..98409500hg18UCSC Ensembl
Innerchr15:98175500..98409500hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38234001
hg19234001
hg18234001
hg17234001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34620
Supporting Variants
SamplesNA19141
Known GenesADAMTS17
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980892
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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