A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986866



Internal ID12980167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9772081..9868101hg38UCSC Ensembl
Innerchr7:9811710..9907730hg19UCSC Ensembl
Innerchr7:9778235..9874255hg18UCSC Ensembl
Innerchr7:9584950..9680970hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3896021
hg1996021
hg1896021
hg1796021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34783
Supporting Variants
SamplesNA18552
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986866
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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