A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598401



Internal ID21790445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39259379..39259379hg38UCSC Ensembl
chr12:39653181..39653181hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598401
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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