A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464864



Internal ID22522752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60131677..60177829hg38UCSC Ensembl
chr11:59899150..59945302hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3846153
hg1946153
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865814
Supporting Variants
Samples
Known GenesMS4A6A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464864
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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