A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525407



Internal ID20898768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:49508734..49510434hg38UCSC Ensembl
chr19:50011991..50013691hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525407
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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