A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517330



Internal ID20890691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64143588..64144090hg38UCSC Ensembl
chr17:62220948..62221450hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517330
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