A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845455



Internal ID22620390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79217039..79219138hg38UCSC Ensembl
chr6:79926756..79928855hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508046
Samples
Known GenesHMGN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845455
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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