A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907847



Internal ID22683057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33530419..33532004hg38UCSC Ensembl
chr9:33530417..33532002hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381586
hg191586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449186
Samples
Known GenesANKRD18B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907847
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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