A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140917



Internal ID20707957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145102857..145104792hg38UCSC Ensembl
chr6:145423993..145425928hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381936
hg191936
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605943
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140917
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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