A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845619



Internal ID22620554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45582886..45584219hg38UCSC Ensembl
chr6:45550623..45551956hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845619
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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