A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837555



Internal ID22612490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106809402..106841907hg38UCSC Ensembl
chr4:107730559..107763064hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3832506
hg1932506
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837555
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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