A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508690



Internal ID20881994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5835181..5840386hg38UCSC Ensembl
chr17:5738501..5743706hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg385206
hg195206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188167
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508690
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