A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842027



Internal ID22616962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24392907..24396306hg38UCSC Ensembl
chr5:24393016..24396415hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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