A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179327



Internal ID20746367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34231901..34236000hg38UCSC Ensembl
chr18:31811865..31815964hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530987
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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