A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616815



Internal ID21808862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120561098..120561098hg38UCSC Ensembl
chr12:120998901..120998901hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091829
Supporting Variants
Samples
Known GenesRNF10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616815
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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