A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14363327



Internal ID22273390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:37248831..37249174hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38344
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222166
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14363327
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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