A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137155



Internal ID20704195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116540131..116548829hg38UCSC Ensembl
chr6:116861294..116869992hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg388699
hg198699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617155
Supporting Variants
Samples
Known GenesFAM26D, TRAPPC3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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