A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714112



Internal ID137778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65127009..65133147hg38UCSC Ensembl
chr17:63123127..63129265hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg386139
hg196139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714112
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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