A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473047



Internal ID21130600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60236845..60304077hg38UCSC Ensembl
chr11:60004318..60071550hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3867233
hg1967233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1201n223
Supporting Variantsnssv17992495
Samples
Known GenesMS4A4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473047
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