A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515947



Internal ID20889308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53672724..53678773hg38UCSC Ensembl
chr19:54175978..54182027hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386050
hg196050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200205
Samples
Known GenesMIR498, MIR520E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515947
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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