A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521993



Internal ID20895354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:606158..635412hg38UCSC Ensembl
chr19:606158..635412hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3829255
hg1929255
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198973
Samples
Known GenesHCN2, POLRMT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521993
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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