A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499689



Internal ID20872912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12206167..12207379hg38UCSC Ensembl
chr17:12109484..12110696hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381213
hg191213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer