A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843006



Internal ID22617941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4656426..4657553hg38UCSC Ensembl
chr5:4656539..4657666hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843006
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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