A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211889



Internal ID20778929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51830001..51854000hg38UCSC Ensembl
chr4:52696167..52720166hg19UCSC Ensembl
Cytoband4q11
Allele length
AssemblyAllele length
hg3824000
hg1924000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6381611
Supporting Variants
Samples
Known GenesDCUN1D4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211889
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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