A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17011155



Internal ID75084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29105663..29118153hg38UCSC Ensembl
chr8:28963180..28975670hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3812491
hg1912491
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559379
Supporting Variants
Samples
Known GenesKIF13B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17011155
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004371


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