A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981764



Internal ID12973901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165391..328070hg38UCSC Ensembl
Innerchr6:165391..328070hg19UCSC Ensembl
Innerchr6:110391..273070hg18UCSC Ensembl
Innerchr6:110391..273070hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38162680
hg19162680
hg18162680
hg17162680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752087
Supporting Variants
SamplesBEC_465
Known GenesDUSP22
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981764
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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