A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139416



Internal ID20706456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134204929..134214168hg38UCSC Ensembl
chr6:134526067..134535306hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg389240
hg199240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609278
Supporting Variants
Samples
Known GenesSGK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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