A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712134



Internal ID135800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21027257..21027335hg38UCSC Ensembl
chr17:20930570..20930648hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514153
Supporting Variants
Samples
Known GenesUSP22
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712134
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.009835


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