A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860229



Internal ID22635164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64089490..64099980hg38UCSC Ensembl
chrUn_gl000211:121043..131533hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3810491
hg1910491
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513958, nssv17513957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860229
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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