A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848490



Internal ID22623425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79425273..79429174hg38UCSC Ensembl
chr15:79717615..79721516hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474214
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848490
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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