A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981665



Internal ID12972487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162965825..163998074hg38UCSC Ensembl
Innerchr3:162683613..163715862hg19UCSC Ensembl
Innerchr3:164166307..165198556hg18UCSC Ensembl
Innerchr3:164166315..165198564hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg381032250
hg191032250
hg181032250
hg171032250
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751982
Supporting Variants
SamplesBEC_314
Known GenesCT64
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981665
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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