A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506474



Internal ID20879754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78152259..78158990hg38UCSC Ensembl
chr15:78444601..78451332hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg386732
hg196732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026756
Samples
Known GenesIDH3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506474
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