A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922538



Internal ID22697763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75348489..75353833hg38UCSC Ensembl
chr9:77963405..77968749hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg385345
hg195345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922538
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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