A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525410



Internal ID20898771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48016783..48017530hg38UCSC Ensembl
chr18:45543154..45543901hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38748
hg19748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525410
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