A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325694



Internal ID22267223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38752113..38752347hg38UCSC Ensembl
chr6:38719889..38720123hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528921
Supporting Variants
SamplesNA19238
Known GenesDNAH8
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325694
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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