A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215897



Internal ID22362070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12013090..12013350hg38UCSC Ensembl
chr10:12055089..12055349hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14329781
SamplesNA19238
Known GenesUPF2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215897
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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