A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732609



Internal ID156275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45335592..45335592hg38UCSC Ensembl
chr20:43964232..43964232hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535923
Supporting Variants
Samples
Known GenesSDC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732609
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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