A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981187



Internal ID12626268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62643000..63245808hg38UCSC Ensembl
Innerchr7:62103378..62706186hg19UCSC Ensembl
Innerchr7:61740813..62343621hg18UCSC Ensembl
Innerchr7:61547528..62150336hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38602809
hg19602809
hg18602809
hg17602809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752164
Supporting Variants
SamplesBEC_361
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981187
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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