A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529590



Internal ID22398982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80357758..80357809hg38UCSC Ensembl
chr8:81269993..81270044hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341160, nssv14341162, nssv14341161
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529590
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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