A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522669



Internal ID20896030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36501211..36523767hg38UCSC Ensembl
chr20:35129614..35152170hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3822557
hg1922557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068052
Samples
Known GenesDLGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522669
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