A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932149



Internal ID22707442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6049842..6049942hg38UCSC Ensembl
chr20:6030488..6030588hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393045
Samples
Known GenesLRRN4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932149
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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