A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522634



Internal ID20895995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22108390..22109438hg38UCSC Ensembl
chr18:19688351..19689399hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381049
hg191049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522634
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