A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531695



Internal ID20905056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61967146..61970000hg38UCSC Ensembl
chr18:59634379..59637233hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg382855
hg192855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531695
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