A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498516



Internal ID20871727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6573831..6599751hg38UCSC Ensembl
chr17:6477151..6503071hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3825921
hg1925921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037858
Samples
Known GenesKIAA0753
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498516
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