A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448731



Internal ID21106284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17854217..17858136hg38UCSC Ensembl
chr11:17875764..17879683hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383920
hg193920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988614
Samples
Known GenesSERGEF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448731
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