A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486233



Internal ID21143786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100938901..100943500hg38UCSC Ensembl
chr13:101591155..101595754hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18006770
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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