A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852759



Internal ID22627694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76641726..76656218hg38UCSC Ensembl
chr15:76934067..76948559hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3814493
hg1914493
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473673
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852759
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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