A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134685



Internal ID20701725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105061609..105073278hg38UCSC Ensembl
chr6:105509484..105521153hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811670
hg1911670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614138
Supporting Variants
Samples
Known GenesLIN28B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134685
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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