A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618481



Internal ID20991552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144758303..144766924hg38UCSC Ensembl
chr6:145079439..145088060hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg388622
hg198622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216936
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618481
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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