A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857198



Internal ID22632133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75179668..75182867hg38UCSC Ensembl
chr9:77794584..77797783hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857198
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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