A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408108



Internal ID21065661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115580866..115581157hg38UCSC Ensembl
chr5:114916563..114916854hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125632
Samples
Known GenesTICAM2, TMED7-TICAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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