A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534738



Internal ID20908099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11329517..11336883hg38UCSC Ensembl
chr19:11440193..11447559hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387367
hg197367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044997
Samples
Known GenesRAB3D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534738
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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