A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982833



Internal ID12975634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32047316..32091516hg38UCSC Ensembl
Innerchr21:33419629..33463829hg19UCSC Ensembl
Innerchr21:32341500..32385700hg18UCSC Ensembl
Innerchr21:32341500..32385700hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3844201
hg1944201
hg1844201
hg1744201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751926
Supporting Variants
SamplesBEC_603
Known GenesLINC00159
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982833
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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