A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861649



Internal ID22636584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5233777..5238413hg38UCSC Ensembl
chr9:5233777..5238413hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg384637
hg194637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513687
Samples
Known GenesINSL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861649
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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