A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520728



Internal ID20894089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29758037..29806824hg38UCSC Ensembl
chr18:27338002..27386789hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3848788
hg1948788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182992
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520728
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