A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141574



Internal ID20708614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15283876..15292186hg38UCSC Ensembl
chr6:15284107..15292417hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388311
hg198311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406302
Supporting Variants
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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