A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503662



Internal ID20876918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96465520..96466495hg38UCSC Ensembl
chr15:97008750..97009725hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027899
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503662
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