A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147627



Internal ID20714667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99296101..99298100hg38UCSC Ensembl
chr6:99743977..99745976hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600841
Supporting Variants
Samples
Known GenesFAXC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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