A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18039394



Internal ID20606434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12361019..12361511hg38UCSC Ensembl
chr18:12361018..12361510hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527967
Supporting Variants
Samples
Known GenesAFG3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18039394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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