A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496746



Internal ID20869949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19761528..19764926hg38UCSC Ensembl
chr17:19664841..19668239hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383399
hg193399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496746
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