A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732398



Internal ID156064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:41277381..41278844hg38UCSC Ensembl
chr20:39906021..39907484hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg381464
hg191464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527081
Supporting Variants
Samples
Known GenesZHX3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.220887


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