A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14313191



Internal ID22126457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:232312112..232312112hg38UCSC Ensembl
chr1:232447858..232447858hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3561943
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14313191
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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