A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523347



Internal ID20896708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41222598..41223213hg38UCSC Ensembl
chr19:41728503..41729118hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198805
Samples
Known GenesAXL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523347
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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