A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220772



Internal ID22365376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26595163..26655522hg38UCSC Ensembl
chr10:26884092..26944451hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3860360
hg1960360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336048, nssv14336047
SamplesNA19239, NA19240
Known GenesLINC00202-2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220772
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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