A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734697



Internal ID158363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33778573..33778877hg38UCSC Ensembl
chr21:35150877..35151181hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543696
Supporting Variants
Samples
Known GenesITSN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.040431


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