A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14371218



Internal ID22276809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73618322..73618631hg38UCSC Ensembl
chr14:74085026..74085335hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529112
Supporting Variants
SamplesNA19239
Known GenesACOT6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14371218
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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