A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188960



Internal ID20756000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:33039610..33424748hg38UCSC Ensembl
chr18:30619574..31004712hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38385139
hg19385139
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524934
Supporting Variants
Samples
Known GenesCCDC178
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188960
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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