A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513563



Internal ID20886908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32399553..32432607hg38UCSC Ensembl
chr17:30726572..30759626hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3833055
hg1933055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191306
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513563
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