A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838288



Internal ID22613223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146392023..146423182hg38UCSC Ensembl
chr4:147313175..147344334hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3831160
hg1931160
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492957
Samples
Known GenesMIR7849, SLC10A7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838288
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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