A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986912



Internal ID21896255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17579458..17579588hg38UCSC Ensembl
chr2:17760725..17760855hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531270
Samples
Known GenesVSNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986912
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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