A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190335



Internal ID20757375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50902383..50938553hg38UCSC Ensembl
chr16:50936294..50972464hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3836171
hg1936171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190335
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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