A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519468



Internal ID20892829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32718681..32722980hg38UCSC Ensembl
chr20:31306483..31310784hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg384300
hg194302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067408
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519468
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