A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532519



Internal ID21856875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31766623..31812664hg38UCSC Ensembl
chr2:31991692..32037733hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3846042
hg1946042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532519
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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