A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656620



Internal ID18608215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76550385..76927895hg38UCSC Ensembl
Innerchr7:76179702..76557212hg19UCSC Ensembl
Innerchr7:76017638..76395148hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38377511
hg19377511
hg18377511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019789
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)nssv3656620
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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