A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732999



Internal ID156665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52496066..52497774hg38UCSC Ensembl
chr20:51112605..51114313hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381709
hg191709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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