A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908191



Internal ID22683401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78561976..78567698hg38UCSC Ensembl
chr9:81176892..81182614hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg385723
hg195723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908191
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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