A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529696



Internal ID22399087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57910056..57910125hg38UCSC Ensembl
chr8:58822615..58822684hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341541
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529696
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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