A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510852



Internal ID20884175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69107128..69116922hg38UCSC Ensembl
chr15:69399468..69409262hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg389795
hg199795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026291
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510852
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