A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216163



Internal ID20783203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17756133..17894798hg38UCSC Ensembl
chr6:17756364..17895029hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38138666
hg19138666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407474
Supporting Variants
Samples
Known GenesKIF13A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216163
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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