A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529637



Internal ID22399029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103001939..103002285hg38UCSC Ensembl
chr8:104014167..104014513hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342215, nssv14342216
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529637
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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