A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838266



Internal ID22613201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139926793..139936278hg38UCSC Ensembl
chr4:140847947..140857432hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg389486
hg199486
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492928
Samples
Known GenesMAML3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838266
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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