A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857437



Internal ID22632372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43003771..43020038hg38UCSC Ensembl
chr9:42963210..42979497hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3816268
hg1916288
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513562, nssv17513563
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857437
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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