A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856582



Internal ID22631517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43621386..43630248hg38UCSC Ensembl
chr15:43913584..43922446hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg388863
hg198863
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv747n209
Supporting Variantsnssv17471844, nssv17471845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856582
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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