A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14330701



Internal ID22263107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105994629..105995953hg38UCSC Ensembl
chr6:106442504..106443828hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeCNV duplication
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202732
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14330701
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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