A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855431



Internal ID22630366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94009761..94012940hg38UCSC Ensembl
chr9:96772043..96775222hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg383180
hg193180
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514801
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855431
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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