A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561201



Internal ID21885556
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 StatusS
Merged Variantsnsv6013040
Supporting Variants
Samples
Known GenesKCND2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561201
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer