A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911979



Internal ID8741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43833663..43833963hg38UCSC Ensembl
chr2:44060802..44061102hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448595
Supporting Variants
Samples
Known GenesABCG5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911979
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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