A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505694



Internal ID20878967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79839841..79868056hg38UCSC Ensembl
chr16:79873738..79901953hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3828216
hg1928216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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