A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864011



Internal ID22638946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74823014..74825663hg38UCSC Ensembl
chr15:75115355..75118004hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473627
Samples
Known GenesLMAN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864011
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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