A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350390



Internal ID21007943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:32301879..32308285hg38UCSC Ensembl
chr2:32526948..32533354hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg386407
hg196407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208205
Samples
Known GenesYIPF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350390
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