A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108983



Internal ID22018216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75975783..75975783hg38UCSC Ensembl
chr18:73687738..73687738hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108983
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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