A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508726



Internal ID20882030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84133065..84181595hg38UCSC Ensembl
chr16:84166670..84215201hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3848531
hg1948532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194732
Samples
Known GenesDNAAF1, HSDL1, TAF1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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