A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986607



Internal ID12635225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:114274957..115136804hg38UCSC Ensembl
Innerchr6:114596121..115457968hg19UCSC Ensembl
Innerchr6:114702814..115564661hg18UCSC Ensembl
Innerchr6:114702814..115564661hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38861848
hg19861848
hg18861848
hg17861848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34434
Supporting Variants
SamplesNA19092
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986607
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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