A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013716



Internal ID76823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66195593..66196477hg38UCSC Ensembl
chr8:67107828..67108712hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554315
Supporting Variants
Samples
Known GenesLINC00967
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013716
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.002966


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