A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14312305



Internal ID22296404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14954991..14955278hg38UCSC Ensembl
chr4:14956615..14956902hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203756
Supporting Variants
SamplesNA19240
Known GenesCPEB2-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14312305
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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