A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612748



Internal ID21804795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87831770..87831770hg38UCSC Ensembl
chr13:88484025..88484025hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094632
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612748
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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