A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193682



Internal ID20760722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:70631665..70665355hg38UCSC Ensembl
chr16:70665568..70699258hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3833691
hg1933691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6506022
Supporting Variants
Samples
Known GenesIL34, MTSS1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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