A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502481



Internal ID20875726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82927901..83065800hg38UCSC Ensembl
chr16:82961506..83099405hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38137900
hg19137900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190897
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502481
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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