A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927191



Internal ID18836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241235917..241236052hg38UCSC Ensembl
chr2:242175332..242175467hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440858
Supporting Variants
Samples
Known GenesHDLBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927191
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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