A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608380



Internal ID21800427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34133667..34141657hg38UCSC Ensembl
chr15:34425868..34433858hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg387991
hg197991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034661
Supporting Variants
Samples
Known GenesKATNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608380
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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