A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226756



Internal ID22369455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95288011..95288071hg38UCSC Ensembl
chr8:96300239..96300299hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341360, nssv14341362, nssv14341359, nssv14341361
SamplesHG00512, HG00732, HG00733, HG00513
Known GenesLOC100616530
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226756
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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