A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988532



Internal ID59783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97049515..97058507hg38UCSC Ensembl
chr6:97497391..97506383hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg388993
hg198993
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563671
Supporting Variants
Samples
Known GenesKLHL32
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988532
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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