A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843560



Internal ID22618495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8701182..8717358hg38UCSC Ensembl
chr5:8701294..8717470hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3816177
hg1916177
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843560
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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