A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532529



Internal ID21856885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:56964251..57098408hg38UCSC Ensembl
chr2:57191386..57325543hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38134158
hg19134158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989582
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532529
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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