A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838735



Internal ID22613670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182200950..182214203hg38UCSC Ensembl
chr4:183122103..183135356hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3813254
hg1913254
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838735
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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