A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526474



Internal ID21850832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162767254..162767254hg38UCSC Ensembl
chr2:163623764..163623764hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042146
Supporting Variants
Samples
Known GenesKCNH7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526474
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