A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983636



Internal ID56468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35766000..35800000hg38UCSC Ensembl
chr6:35733777..35767777hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3834001
hg1934001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140939
Supporting Variants
Samples
Known GenesCLPS, CLPSL1, CLPSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983636
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012086


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