A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518442



Internal ID20891803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52275815..52278475hg38UCSC Ensembl
chr19:52779068..52781728hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg382661
hg192661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048774
Samples
Known GenesZNF766
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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