A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14328880



Internal ID22322668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102293688..102293816hg38UCSC Ensembl
chr6:102741563..102741691hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529852
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14328880
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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