A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3755341



Internal ID18706936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76506401..76977978hg38UCSC Ensembl
Innerchr7:76135718..76607295hg19UCSC Ensembl
Innerchr7:75973654..76445231hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38471578
hg19471578
hg18471578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034943
Supporting Variants
Samples
Known GenesLOC100133091, 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)nssv3755341
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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