A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508615



Internal ID20881919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5797363..5804449hg38UCSC Ensembl
chr17:5700683..5707769hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387087
hg197087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036282
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508615
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