A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331232



Internal ID22279140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151373612..151373840hg38UCSC Ensembl
chr6:151694747..151694975hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191156
Supporting Variants
SamplesNA19239
Known GenesZBTB2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331232
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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