A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912592



Internal ID22687808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60766156..60767967hg38UCSC Ensembl
chr11:60533629..60535440hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355508
Samples
Known GenesMS4A15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912592
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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