A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990257



Internal ID12632110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35233169..35887724hg38UCSC Ensembl
Innerchr16:34467540..35122095hg19UCSC Ensembl
Innerchr16:34325041..34979596hg18UCSC Ensembl
Innerchr16:34325041..34979596hg17UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38654556
hg19654556
hg18654556
hg17654556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34862
Supporting Variants
SamplesNA12004
Known GenesFLJ26245, LOC100130700, LOC146481, LOC283914
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990257
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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