A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986278



Internal ID12975621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32047358..32091533hg38UCSC Ensembl
Innerchr21:33419671..33463846hg19UCSC Ensembl
Innerchr21:32341542..32385717hg18UCSC Ensembl
Innerchr21:32341542..32385717hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3844176
hg1944176
hg1844176
hg1744176
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)essv6986278
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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