A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012293



Internal ID21921636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29113723..29113891hg38UCSC Ensembl
chr8:28971240..28971408hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562707
Samples
Known GenesKIF13B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012293
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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