A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526759



Internal ID20900120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45736802..45742168hg38UCSC Ensembl
chr19:46240060..46245426hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg385367
hg195367
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198900
Samples
Known GenesLOC388553
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526759
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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