A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189582



Internal ID20756622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22813734..23250365hg38UCSC Ensembl
chr11:22835280..23271911hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38436632
hg19436632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455447
Supporting Variants
Samples
Known GenesCCDC179, SVIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189582
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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