A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331641



Internal ID22209530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113996129..113996181hg38UCSC Ensembl
chr6:114317293..114317345hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201172
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331641
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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