A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889842



Internal ID22664863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139926731..139936051hg38UCSC Ensembl
chr4:140847885..140857205hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg389321
hg199321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423053
Samples
Known GenesMAML3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889842
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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