A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187559



Internal ID20754599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76815331..77199738hg38UCSC Ensembl
chr16:76849228..77233635hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38384408
hg19384408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496671
Supporting Variants
Samples
Known GenesMIR4719, MON1B, SYCE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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