A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927616



Internal ID19125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191130355..191133929hg38UCSC Ensembl
chr2:191995081..191998655hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg383575
hg193575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453169
Supporting Variants
Samples
Known GenesSTAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927616
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01842


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