A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221185



Internal ID22365656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100376101..100376167hg38UCSC Ensembl
chr10:102135858..102135924hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1031n152
Supporting Variantsnssv14352941, nssv14352940, nssv14352942
SamplesNA19238, NA19239, NA19240
Known GenesLINC00263
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221185
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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