A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293638



Internal ID20502856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97482694..97482694hg38UCSC Ensembl
chr12:97876472..97876472hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761049
Supporting Variants
Samples
Known GenesRMST
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293638
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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