A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6494040



Internal ID21151593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48579638..48585420hg38UCSC Ensembl
chr13:49153774..49159556hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg385783
hg195783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009381
Samples
Known GenesLINC00462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6494040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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