A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138994



Internal ID20706034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13938307..13939800hg38UCSC Ensembl
chr6:13938538..13940031hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381494
hg191494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396409
Supporting Variants
Samples
Known GenesRNF182
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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