A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537176



Internal ID21861531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144743072..144749577hg38UCSC Ensembl
chr2:145500639..145507144hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg386506
hg196506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986314
Supporting Variants
Samples
Known GenesTEX41
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537176
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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