A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845526



Internal ID22620461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48129105..48133051hg38UCSC Ensembl
chr6:48096841..48100787hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg383947
hg193947
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845526
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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