A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020833



Internal ID21930176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34153768..34154351hg38UCSC Ensembl
chr15:34445969..34446552hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601770
Samples
Known GenesKATNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020833
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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