A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838791



Internal ID22613726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181085796..181087295hg38UCSC Ensembl
chr4:182006949..182008448hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491292
Samples
Known GenesLINC00290
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838791
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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