A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751560



Internal ID12985112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35203218..35499505hg38UCSC Ensembl
Innerchr16:34437589..34733876hg19UCSC Ensembl
Innerchr16:34295090..34591377hg18UCSC Ensembl
Innerchr16:34295090..34591377hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38296288
hg19296288
hg18296288
hg17296288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv117e55
Supporting Variantsessv6982536, essv6982535
SamplesBEC_565
Known GenesLOC146481, LOC283914
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751560
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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