A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987784



Internal ID12978319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:84673533..84851633hg38UCSC Ensembl
Innerchr7:84302849..84480949hg19UCSC Ensembl
Innerchr7:84140785..84318885hg18UCSC Ensembl
Innerchr7:83947500..84125600hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38178101
hg19178101
hg18178101
hg17178101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34238
Supporting Variants
SamplesNA10831
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987784
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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