A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137317



Internal ID20704357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118090880..118093778hg38UCSC Ensembl
chr6:118412043..118414941hg19UCSC Ensembl
Cytoband6q22.2
Allele length
AssemblyAllele length
hg382899
hg192899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600131
Supporting Variants
Samples
Known GenesSLC35F1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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