A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864434



Internal ID22639369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85797291..85801284hg38UCSC Ensembl
chr15:86340522..86344515hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383994
hg193994
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864434
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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