A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528230



Internal ID22397616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61122800..61123326hg38UCSC Ensembl
chr8:62035359..62035885hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38527
hg19527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342254, nssv14342253
SamplesNA19239, HG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528230
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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