A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656530



Internal ID18608125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76479432..77136114hg38UCSC Ensembl
Innerchr7:76108749..76765431hg19UCSC Ensembl
Innerchr7:75946685..76603367hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38656683
hg19656683
hg18656683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022820
Supporting Variants
Samples
Known GenesCCDC146, DTX2, DTX2P1-UPK3BP1-PMS2P11, LOC100132832, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656530
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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