A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405031



Internal ID21062584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12039183..12255228hg38UCSC Ensembl
chr6:12039416..12255461hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38216046
hg19216046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214567
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405031
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