A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519171



Internal ID20892532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11363022..11366530hg38UCSC Ensembl
chr19:11473698..11477206hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg383509
hg193509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198063
Samples
Known GenesLPPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519171
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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