A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861542



Internal ID22636477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73052914..73055333hg38UCSC Ensembl
chr9:75667830..75670249hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382420
hg192420
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514256, nssv17514257
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861542
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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