A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724870



Internal ID148536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60161678..60167768hg38UCSC Ensembl
chr17:58239039..58245129hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg386091
hg196091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724870
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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