A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516005



Internal ID20889366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19518498..19571449hg38UCSC Ensembl
chr19:19629307..19682258hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3852952
hg1952952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198375
Samples
Known GenesCILP2, NDUFA13, PBX4, YJEFN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516005
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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