A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379982



Internal ID22266585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80911975..80913525hg38UCSC Ensembl
chr15:81204316..81205866hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381551
hg191551
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3558880
Supporting Variants
SamplesNA19238
Known GenesKIAA1199
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379982
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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