A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512388



Internal ID20885722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96686878..96698648hg38UCSC Ensembl
chr15:97230108..97241878hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3811771
hg1911771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512388
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