A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570219



Internal ID21762262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96927485..96927485hg38UCSC Ensembl
chr6:97375361..97375361hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064172
Supporting Variants
Samples
Known GenesKLHL32
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570219
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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