A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922441



Internal ID22697666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36555109..36561720hg38UCSC Ensembl
chr9:36555106..36561717hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg386612
hg196612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922441
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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