A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516205



Internal ID20889566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50337535..50362272hg38UCSC Ensembl
chr19:50840792..50865529hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3824738
hg1924738
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198277
Samples
Known GenesNAPSA, NAPSB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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