A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843990



Internal ID22618925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109687629..109693728hg38UCSC Ensembl
chr6:110008832..110014931hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500910
Samples
Known GenesAK9, FIG4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843990
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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