A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14327873



Internal ID22282046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74543279..74543337hg38UCSC Ensembl
chr6:75252995..75253053hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191205
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14327873
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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