A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728863



Internal ID152529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37730655..37734253hg38UCSC Ensembl
chr22:38126662..38130260hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383599
hg193599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538329
Supporting Variants
Samples
Known GenesTRIOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728863
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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