A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838327



Internal ID22613262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1585462..1601200hg38UCSC Ensembl
chr4:1587189..1602927hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3815739
hg1915739
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838327
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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