A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527619



Internal ID20900980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:64788185..64883919hg38UCSC Ensembl
chr18:62455421..62551155hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3895735
hg1995735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18042635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527619
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