A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924596



Internal ID22699823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106977212..106979770hg38UCSC Ensembl
chr9:109739493..109742051hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430150
Samples
Known GenesMIR548Q, ZNF462
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924596
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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