A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520373



Internal ID20893734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40740805..40746297hg38UCSC Ensembl
chr19:41246710..41252202hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg385493
hg195493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047770
Samples
Known GenesC19orf54, ITPKC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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