A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732297



Internal ID155963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38266522..38359675hg38UCSC Ensembl
chr20:36894924..36988329hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3893154
hg1993406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520033
Supporting Variants
Samples
Known GenesBPI, LBP, LOC149684
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732297
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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