A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988963



Internal ID12984258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36136332..36239632hg38UCSC Ensembl
Innerchr21:37508630..37611930hg19UCSC Ensembl
Innerchr21:36430500..36533800hg18UCSC Ensembl
Innerchr21:36430500..36533800hg17UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38103301
hg19103301
hg18103301
hg17103301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751928
Supporting Variants
SamplesSPC_86
Known GenesCBR3, CBR3-AS1, DOPEY2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988963
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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