A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714211



Internal ID137877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68260507..68264066hg38UCSC Ensembl
chr17:66256648..66260207hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg383560
hg193560
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554220
Supporting Variants
Samples
Known GenesARSG
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714211
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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