A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520560



Internal ID20893921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22164801..22167600hg38UCSC Ensembl
chr18:19744762..19747561hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040285
Samples
Known GenesGATA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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