A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924724



Internal ID22699951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132514046..132514128hg38UCSC Ensembl
chr9:135389433..135389515hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434376
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924724
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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