A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593058



Internal ID21785101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99362345..99362345hg38UCSC Ensembl
chr9:102124627..102124627hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38246
hg19246
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089284
Supporting Variants
Samples
Known GenesNAMA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593058
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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