A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216019



Internal ID20783059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135520397..135732537hg38UCSC Ensembl
chr6:135841535..136053675hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38212141
hg19212141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604802
Supporting Variants
Samples
Known GenesLINC00271
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216019
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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