A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14372205



Internal ID22229611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76347430..76347865hg38UCSC Ensembl
chr14:76813773..76814208hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38436
hg19436
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527247
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14372205
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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