A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713802



Internal ID137468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58254147..58254223hg38UCSC Ensembl
chr17:56331508..56331584hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538538
Supporting Variants
Samples
Known GenesLPO
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713802
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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