A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536397



Internal ID20909745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:14658501..14667100hg38UCSC Ensembl
chr21:16030822..16039421hg19UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4550n223
Supporting Variantsnssv18203766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536397
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