A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14385346



Internal ID22277348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76189283..76189359hg38UCSC Ensembl
chr15:76481624..76481700hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3224947
Supporting Variants
SamplesNA19239
Known GenesC15orf27
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14385346
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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