A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501643



Internal ID20874880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77440501..77442800hg38UCSC Ensembl
chr15:77732843..77735142hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025495
Samples
Known GenesHMG20A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501643
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