A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524776



Internal ID20898137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11338936..11343172hg38UCSC Ensembl
chr19:11449612..11453848hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384237
hg194237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044999
Samples
Known GenesRAB3D, TMEM205
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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