A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921253



Internal ID22696476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97911064..97911776hg38UCSC Ensembl
chr9:100673346..100674058hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448280
Samples
Known GenesC9orf156
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921253
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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