A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534752



Internal ID20908113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51023416..51038767hg38UCSC Ensembl
chr19:51526672..51542024hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3815352
hg1915353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198295
Samples
Known GenesKLK11, KLK12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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