A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380214



Internal ID22174157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68883663..68884073hg38UCSC Ensembl
chr15:69176002..69176412hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217185
Supporting Variants
SamplesHG00514
Known GenesMIR548H4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380214
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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