A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981763



Internal ID12973890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:165391..285695hg38UCSC Ensembl
Innerchr6:165391..285695hg19UCSC Ensembl
Innerchr6:110391..230695hg18UCSC Ensembl
Innerchr6:110391..230695hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38120305
hg19120305
hg18120305
hg17120305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752087
Supporting Variants
SamplesBEC_465
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981763
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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