A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859684



Internal ID22634619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75296833..75301781hg38UCSC Ensembl
chr15:75589174..75594122hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg384949
hg194949
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473637, nssv17472309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859684
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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