A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844834



Internal ID22619769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23101223..23104470hg38UCSC Ensembl
chr6:23101451..23104698hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383248
hg193248
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844834
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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