A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027552



Internal ID86072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97271205..97271520hg38UCSC Ensembl
chr9:100033487..100033802hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486843
Supporting Variants
Samples
Known GenesLOC100499484, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027552
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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