A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181496



Internal ID20748536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30776925..30884274hg38UCSC Ensembl
chr11:30798472..30905821hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38107350
hg19107350
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445519
Supporting Variants
Samples
Known GenesDCDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00025


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