A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714209



Internal ID137875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68219185..68219270hg38UCSC Ensembl
chr17:66215326..66215411hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554808
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714209
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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