A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927147



Internal ID18808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240960033..240960111hg38UCSC Ensembl
chr2:241899450..241899528hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452501
Supporting Variants
Samples
Known GenesLOC200772
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927147
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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