A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838359



Internal ID22613294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153370444..153372543hg38UCSC Ensembl
chr4:154291596..154293695hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1605n209
Supporting Variantsnssv17492978, nssv17499702
Samples
Known GenesMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838359
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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