A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656551



Internal ID18608146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76506401..77083484hg38UCSC Ensembl
Innerchr7:76135718..76712801hg19UCSC Ensembl
Innerchr7:75973654..76550737hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38577084
hg19577084
hg18577084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033494
Supporting Variants
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832, 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)nssv3656551
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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