A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14370171



Internal ID22266683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31408914..31409055hg38UCSC Ensembl
chr14:31878120..31878261hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211701
Supporting Variants
SamplesNA19238
Known GenesHEATR5A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14370171
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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