A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515467



Internal ID20888827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77951337..78630216hg38UCSC Ensembl
chr16:77985234..78664113hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38678880
hg19678880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2942n223
Supporting Variantsnssv18189858
Samples
Known GenesCLEC3A, VAT1L, WWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515467
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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