A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140181



Internal ID20707221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14281624..14286245hg38UCSC Ensembl
chr6:14281855..14286476hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg384622
hg194622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398300
Supporting Variants
Samples
Known GenesLINC01108
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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