A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216958



Internal ID20783998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146508341..146554053hg38UCSC Ensembl
chr6:146829477..146875189hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3845713
hg1945713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601173
Supporting Variants
Samples
Known GenesRAB32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216958
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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