A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510800



Internal ID20884123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67850581..67857911hg38UCSC Ensembl
chr15:68142919..68150249hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387331
hg197331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510800
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