A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862786



Internal ID22637721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74856350..74859272hg38UCSC Ensembl
chr15:75148691..75151613hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382923
hg192923
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473630
Samples
Known GenesSCAMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862786
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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