A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013040



Internal ID21922383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120504040..120670315hg38UCSC Ensembl
chr7:120144094..120310369hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38166276
hg19166276
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561201
Samples
Known GenesKCND2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013040
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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