A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986004



Internal ID12982513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44813678..44975984hg38UCSC Ensembl
Innerchr15:45105876..45268182hg19UCSC Ensembl
Innerchr15:42893168..43055474hg18UCSC Ensembl
Innerchr15:42893168..43055474hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38162307
hg19162307
hg18162307
hg17162307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34494
Supporting Variants
SamplesNA19202
Known GenesC15orf43
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986004
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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