A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216935



Internal ID20783975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144684064..144786301hg38UCSC Ensembl
chr6:145005200..145107437hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38102238
hg19102238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605440
Supporting Variants
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216935
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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