A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526904



Internal ID20900265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16124142..16124752hg38UCSC Ensembl
chr19:16234952..16235562hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38611
hg19611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044465
Samples
Known GenesRAB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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