A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359624



Internal ID21017177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157724901..157731600hg38UCSC Ensembl
chr3:157442690..157449389hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359624
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