A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17724818



Internal ID148484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56823567..56827424hg38UCSC Ensembl
chr17:54900928..54904785hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg383858
hg193858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522075
Supporting Variants
Samples
Known GenesC17orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17724818
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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