A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34358



Internal ID12643711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76514332..76936433hg38UCSC Ensembl
Innerchr7:76143649..76565750hg19UCSC Ensembl
Innerchr7:75981585..76403686hg18UCSC Ensembl
Innerchr7:75788300..76210401hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38422102
hg19422102
hg18422102
hg17422102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv234e55
Supporting Variantsessv6986982, essv6979962
SamplesNA18863
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34358
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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