A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732907



Internal ID156573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50904211..50904249hg38UCSC Ensembl
chr20:49520748..49520786hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539230
Supporting Variants
Samples
Known GenesADNP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732907
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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