A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513946



Internal ID20887295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59784219..59831445hg38UCSC Ensembl
chr15:60076418..60123644hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3847227
hg1947227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513946
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