A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845566



Internal ID22620501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57528101..57540026hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3811926
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845566
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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