A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14373768



Internal ID22278256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80900104..80900677hg38UCSC Ensembl
chr15:81192445..81193018hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223556
Supporting Variants
SamplesNA19239
Known GenesKIAA1199
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14373768
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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