A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460305



Internal ID21117858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74463013..74463364hg38UCSC Ensembl
chr11:74174058..74174409hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993603
Samples
Known GenesKCNE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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