A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196227



Internal ID20763267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10606101..10609200hg38UCSC Ensembl
chr18:10606098..10609197hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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