A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656522



Internal ID18608117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76479432..76673974hg38UCSC Ensembl
Innerchr7:76108749..76303291hg19UCSC Ensembl
Innerchr7:75946685..76141227hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38194543
hg19194543
hg18194543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022815
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)nssv3656522
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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