A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223708



Internal ID22367396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94764576..94764744hg38UCSC Ensembl
chr8:95776804..95776972hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342810, nssv14342811
SamplesHG00731, HG00732
Known GenesDPY19L4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223708
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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