A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517087



Internal ID20890448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8373430..8378131hg38UCSC Ensembl
chr19:8438314..8443015hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384702
hg194702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050047
Samples
Known GenesANGPTL4, RAB11B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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