A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988693



Internal ID12629934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20293033..20411418hg38UCSC Ensembl
Innerchr15:20498286..20616671hg19UCSC Ensembl
Innerchr15:18758300..18876685hg18UCSC Ensembl
Innerchr15:18758300..18876685hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38118386
hg19118386
hg18118386
hg17118386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34600
Supporting Variants
SamplesBEC_675
Known GenesHERC2P3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988693
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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