A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319909



Internal ID20853006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22701099..22741834hg38UCSC Ensembl
chr1:23027592..23068327hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3840736
hg1940736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202715
Samples
Known GenesEPHB2, MIR4684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319909
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