A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138543



Internal ID20705583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140187194..140196235hg38UCSC Ensembl
chr6:140508331..140517372hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg389042
hg199042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138543
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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