A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847843



Internal ID22622778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133258636..133260835hg38UCSC Ensembl
chr9:136134027..136136238hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg382200
hg192212
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511673
Samples
Known GenesABO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847843
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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