A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528296



Internal ID22397682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133502724..133502804hg38UCSC Ensembl
chr6:133823862..133823942hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331759
SamplesHG00513
Known GenesEYA4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528296
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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