A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990477



Internal ID12978354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62643000..63445751hg38UCSC Ensembl
Innerchr7:62103378..62906129hg19UCSC Ensembl
Innerchr7:61740813..62543564hg18UCSC Ensembl
Innerchr7:61547528..62350279hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38802752
hg19802752
hg18802752
hg17802752
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35096
Supporting Variants
SamplesNA10839
Known GenesLOC100287704, LOC100287834, ZNF733P
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990477
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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