A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320230



Internal ID20853328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25382801..25394900hg38UCSC Ensembl
chr1:25709292..25721391hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv133n223
Supporting Variantsnssv18202838
Samples
Known GenesRHCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320230
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