A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029796



Internal ID18772327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65034556..65837709hg38UCSC Ensembl
Innerchr7:64494934..65302696hg19UCSC Ensembl
Innerchr7:64132369..64940131hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38803154
hg19807763
hg18807763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655508
Samples
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029796
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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