A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480354



Internal ID21137907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38572071..38572581hg38UCSC Ensembl
chr13:39146208..39146718hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008625
Samples
Known GenesLINC00366
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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