A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513786



Internal ID20887134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6853147..6960047hg38UCSC Ensembl
chr17:6756466..6863366hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38106901
hg19106901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2991n223
Supporting Variantsnssv18037545
Samples
Known GenesALOX12P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513786
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