A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597057



Internal ID21789100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97610159..97610159hg38UCSC Ensembl
chr10:99369916..99369916hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090983
Supporting Variants
Samples
Known GenesHOGA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597057
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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