A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713890



Internal ID137556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59654408..59654711hg38UCSC Ensembl
chr17:57731769..57732072hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146121
Supporting Variants
Samples
Known GenesCLTC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713890
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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