A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439675



Internal ID21097228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31718271..31740822hg38UCSC Ensembl
chr11:31739819..31762370hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3822552
hg1922552
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182209
Samples
Known GenesELP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439675
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