A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984234



Internal ID12631222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65303814..65453065hg38UCSC Ensembl
Innerchr7:64768741..64917978hg19UCSC Ensembl
Innerchr7:64406176..64555413hg18UCSC Ensembl
Innerchr7:64212891..64362128hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38149252
hg19149238
hg18149238
hg17149238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752166
Supporting Variants
SamplesBEC_814
Known GenesZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984234
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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