A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517617



Internal ID21841976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17578569..17578633hg38UCSC Ensembl
chr2:17759836..17759900hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987278
Supporting Variants
Samples
Known GenesVSNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517617
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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