A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732094



Internal ID155760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34402227..34402278hg38UCSC Ensembl
chr20:32990033..32990084hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556339
Supporting Variants
Samples
Known GenesITCH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732094
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002349


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