A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433915



Internal ID21395917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156153721..156158805hg38UCSC Ensembl
chr3:155871510..155876594hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg385085
hg195085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748832
SamplesMDQ045
Known GenesKCNAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433915
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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