A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216020



Internal ID20783060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135668635..135676902hg38UCSC Ensembl
chr6:135989773..135998040hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388268
hg198268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619753
Supporting Variants
Samples
Known GenesLINC00271
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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