A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978129



Internal ID12978682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21200164..21337247hg38UCSC Ensembl
Innerchr3:21241656..21378739hg19UCSC Ensembl
Innerchr3:21216660..21353743hg18UCSC Ensembl
Innerchr3:21216660..21353743hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38137084
hg19137084
hg18137084
hg17137084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35115
Supporting Variants
SamplesNA11881
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978129
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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