A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236456



Internal ID20803496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35765577..35783680hg38UCSC Ensembl
chr6:35733354..35751457hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3818104
hg1918104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410256
Supporting Variants
Samples
Known GenesCLPSL1, CLPSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236456
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00061


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