A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008880



Internal ID21918223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97240419..97240489hg38UCSC Ensembl
chr9:100002701..100002771hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597017
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008880
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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