A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481875



Internal ID21139428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61218202..61222009hg38UCSC Ensembl
chr13:61792336..61796143hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg383808
hg193808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481875
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