A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865552



Internal ID22640487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76508223..76515692hg38UCSC Ensembl
chr15:76800564..76808033hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg387470
hg197470
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473659
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865552
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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