A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204337



Internal ID22353203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134282504..134283298hg38UCSC Ensembl
chr6:134603642..134604436hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331785
SamplesNA19238
Known GenesSGK1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204337
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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