A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500072



Internal ID20873297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101229535..101241389hg38UCSC Ensembl
chr15:101769740..101781594hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3811855
hg1911855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022965
Samples
Known GenesCHSY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500072
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