A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981022



Internal ID12972682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3381816..3670556hg38UCSC Ensembl
Innerchr3:3423500..3712240hg19UCSC Ensembl
Innerchr3:3398500..3687240hg18UCSC Ensembl
Innerchr3:3398500..3687240hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38288741
hg19288741
hg18288741
hg17288741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752000
Supporting Variants
SamplesBEC_337
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981022
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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