A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601770



Internal ID21793817
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 StatusS
Merged Variantsnsv6020833
Supporting Variants
Samples
Known GenesKATNBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601770
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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