A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476170



Internal ID253787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97596188..97658373hg38UCSC Ensembl
chr9:100358470..100420655hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3862186
hg1962186
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027572
Samples
Known GenesNCBP1, TMOD1, TSTD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476170
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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