A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664229



Internal ID18962510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135447160..135508712hg38UCSC Ensembl
Innerchr7:135131908..135193460hg19UCSC Ensembl
Innerchr7:134782448..134844000hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3861553
hg1961553
hg1861553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019101
Supporting Variants
Samples
Known GenesCNOT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3664229
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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