A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189948



Internal ID20756988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34188201..34212900hg38UCSC Ensembl
chr16:33990668..34015367hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3824700
hg1924700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.49585


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