A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14325901



Internal ID22283996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3310263..3310348hg38UCSC Ensembl
chr6:3310497..3310582hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194314
Supporting Variants
SamplesNA19239
Known GenesSLC22A23
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14325901
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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