A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115116



Internal ID21298382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15167096..15170258hg38UCSC Ensembl
Innerchr10:15209095..15212257hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383163
hg193163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089802
Samplessample348
Known GenesNMT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115116
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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