A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457370



Internal ID21114923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60413517..60414072hg38UCSC Ensembl
chr11:60180990..60181545hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992506
Samples
Known GenesMS4A14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457370
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