A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923568



Internal ID16484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:194196033..194352775hg38UCSC Ensembl
chr2:195060757..195217499hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38156743
hg19156743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923568
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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