A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865234



Internal ID22640169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48109896..48111018hg38UCSC Ensembl
chr15:48402093..48403215hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471940, nssv17471939
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865234
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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