A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838056



Internal ID22612991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148147638..148148737hg38UCSC Ensembl
chr4:149068789..149069888hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499666
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838056
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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