A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520854



Internal ID20894215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8978519..9051966hg38UCSC Ensembl
chr19:9089195..9162642hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3873448
hg1973448
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199084
Samples
Known GenesMUC16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520854
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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