A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524738



Internal ID21849096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105950042..105950169hg38UCSC Ensembl
chr2:106566498..106566625hg19UCSC Ensembl
Cytoband2q12.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5985331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524738
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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