A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521581



Internal ID21845940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15678997..15679208hg38UCSC Ensembl
chr2:15819121..15819332hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986962
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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