A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525293



Internal ID21849651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65673025..65673025hg38UCSC Ensembl
chr2:65900159..65900159hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525293
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