A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522193



Internal ID20895554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:21185738..21215144hg38UCSC Ensembl
chr19:21368541..21397946hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3829407
hg1929406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047297
Samples
Known GenesZNF431
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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