A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14371946



Internal ID22124402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57079802..57079982hg38UCSC Ensembl
chr14:57546520..57546700hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529292
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14371946
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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