A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579338



Internal ID21771381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97398035..97398353hg38UCSC Ensembl
chr10:99157792..99158110hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000766
Supporting Variants
Samples
Known GenesRRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579338
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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