A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492153



Internal ID21149706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100405853..100416864hg38UCSC Ensembl
chr13:101058107..101069118hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3811012
hg1911012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184344
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492153
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