A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221117



Internal ID20788157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24372265..24384132hg38UCSC Ensembl
chr6:24372493..24384360hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3811868
hg1911868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398901
Supporting Variants
Samples
Known GenesDCDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221117
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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