A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16931929



Internal ID22014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42817621..42817659hg38UCSC Ensembl
chr3:42859113..42859151hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559487
Supporting Variants
Samples
Known GenesACKR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16931929
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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