A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332113



Internal ID22128866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165839783..165839977hg38UCSC Ensembl
chr6:166253271..166253465hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196968
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332113
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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