A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330819



Internal ID22205246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108201934..108202414hg38UCSC Ensembl
chr6:108523138..108523618hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196249
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330819
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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