A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521509



Internal ID21845868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143801160..143801310hg38UCSC Ensembl
chr2:144558729..144558879hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521509
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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