A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528527



Internal ID20901888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15217060..15221919hg38UCSC Ensembl
chr19:15327871..15332730hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg384860
hg194860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528527
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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