A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194366



Internal ID20761406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36058001..36091500hg38UCSC Ensembl
chr18:33637964..33671463hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3833500
hg1933500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527171
Supporting Variants
Samples
Known GenesRPRD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194366
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00107


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