A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592398



Internal ID21784441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6090877..6090877hg38UCSC Ensembl
chr10:6132840..6132840hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6098217
Supporting Variants
Samples
Known GenesRBM17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592398
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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