A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978368



Internal ID12635168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17092336..17391136hg38UCSC Ensembl
Innerchr7:17131960..17430760hg19UCSC Ensembl
Innerchr7:17098485..17397285hg18UCSC Ensembl
Innerchr7:16905200..17204000hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38298801
hg19298801
hg18298801
hg17298801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34717
Supporting Variants
SamplesNA19007
Known GenesAHR
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978368
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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