A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523162



Internal ID20896523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73356832..73370875hg38UCSC Ensembl
chr18:71024067..71038110hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3814044
hg1914044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523162
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