A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978777



Internal ID12632398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35252528..35468128hg38UCSC Ensembl
Innerchr16:34486899..34702499hg19UCSC Ensembl
Innerchr16:34344400..34560000hg18UCSC Ensembl
Innerchr16:34344400..34560000hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38215601
hg19215601
hg18215601
hg17215601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34629
Supporting Variants
SamplesNA12239
Known GenesLOC283914
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978777
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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