A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522023



Internal ID20895384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50983034..51013511hg38UCSC Ensembl
chr19:51486290..51516767hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3830478
hg1930478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198294
Samples
Known GenesKLK10, KLK7, KLK8, KLK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522023
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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