A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609516



Internal ID21801563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64190018..64190084hg38UCSC Ensembl
chr15:64482217..64482283hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024771
Supporting Variants
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609516
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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