A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497658



Internal ID20870866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72320375..72333200hg38UCSC Ensembl
chr15:72612716..72625541hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3812826
hg1912826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497658
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