A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139729



Internal ID20706769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15460992..15466017hg38UCSC Ensembl
chr6:15461223..15466248hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385026
hg195026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406346
Supporting Variants
Samples
Known GenesJARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139729
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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