A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524518



Internal ID20897879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68692994..68828709hg38UCSC Ensembl
chr18:66360231..66495946hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38135716
hg19135716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197612
Samples
Known GenesCCDC102B, TMX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524518
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer