A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843452



Internal ID22618387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8492964..8511694hg38UCSC Ensembl
chr5:8493077..8511806hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3818731
hg1918730
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17498835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843452
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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