A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941669



Internal ID28471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159735131..159736097hg38UCSC Ensembl
chr3:159452920..159453886hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444312
Supporting Variants
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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