A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475142



Internal ID21132695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60437001..60556000hg38UCSC Ensembl
chr11:60204474..60323473hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38119000
hg19119000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187946
Samples
Known GenesMS4A1, MS4A12, MS4A13, MS4A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475142
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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