A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902623



Internal ID22677783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138310948..138314041hg38UCSC Ensembl
chr4:139232102..139235195hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg383094
hg193094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423403
Samples
Known GenesLINC00499
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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