A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922900



Internal ID22698125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60067824..60067962hg38UCSC Ensembl
chr11:59835297..59835435hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362848
Samples
Known GenesMS4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922900
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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