A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352824



Internal ID21010377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5330577..5372146hg38UCSC Ensembl
chr2:5470710..5512279hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3841570
hg1941570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352824
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