A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482452



Internal ID21140005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63597701..63717500hg38UCSC Ensembl
chr13:64171834..64291633hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38119800
hg19119800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190823
Samples
Known GenesLINC00395
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482452
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer