A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656518



Internal ID18608113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76479432..76653583hg38UCSC Ensembl
Innerchr7:76108749..76282900hg19UCSC Ensembl
Innerchr7:75946685..76120836hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38174152
hg19174152
hg18174152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018487
Supporting Variants
Samples
Known GenesDTX2, 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)nssv3656518
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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