A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988340



Internal ID12635704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76650632..76920732hg38UCSC Ensembl
Innerchr7:76279949..76550049hg19UCSC Ensembl
Innerchr7:76117885..76387985hg18UCSC Ensembl
Innerchr7:75924600..76194700hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38270101
hg19270101
hg18270101
hg17270101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34614
Supporting Variants
SamplesNA19161
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988340
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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