A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222450



Internal ID22366523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100472075..100472268hg38UCSC Ensembl
chr10:102231832..102232025hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352954, nssv14352953
SamplesNA19238, HG00513
Known GenesWNT8B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222450
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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