A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656641



Internal ID18608236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76550385..76967575hg38UCSC Ensembl
Innerchr7:76179702..76596892hg19UCSC Ensembl
Innerchr7:76017638..76434828hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38417191
hg19417191
hg18417191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022999
Supporting Variants
Samples
Known GenesLOC100133091, POMZP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656641
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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