A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183228



Internal ID20750268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37150001..37155800hg38UCSC Ensembl
chr13:37724138..37729937hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477040
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00108


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