A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978366



Internal ID12635170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17092311..17287119hg38UCSC Ensembl
Innerchr7:17131935..17326743hg19UCSC Ensembl
Innerchr7:17098460..17293268hg18UCSC Ensembl
Innerchr7:16905175..17099983hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38194809
hg19194809
hg18194809
hg17194809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34717
Supporting Variants
SamplesNA19007
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978366
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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