A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14389436



Internal ID22128880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91497362..91505513hg38UCSC Ensembl
chr15:92040592..92048743hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg388152
hg198152
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3241790
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14389436
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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