A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983298



Internal ID12976068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9583642..9660952hg38UCSC Ensembl
Innerchr16:9677499..9754809hg19UCSC Ensembl
Innerchr16:9585000..9662310hg18UCSC Ensembl
Innerchr16:9585000..9662310hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3877311
hg1977311
hg1877311
hg1777311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751617
Supporting Variants
SamplesBEC_636
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983298
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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