A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617091



Internal ID21809138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64302198..64302274hg38UCSC Ensembl
chr15:64594397..64594473hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034319
Supporting Variants
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617091
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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