A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848121



Internal ID22623056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72411788..72417072hg38UCSC Ensembl
chr15:72704129..72709413hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg385285
hg195285
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473601, nssv17471775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848121
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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