A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866250



Internal ID22641185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6352532..6353540hg38UCSC Ensembl
chr9:6352532..6353540hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513850, nssv17513849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866250
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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