A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115770



Internal ID21299036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15164477..15170258hg38UCSC Ensembl
Innerchr10:15206476..15212257hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385782
hg195782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089805
Samplessample349
Known GenesNMT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115770
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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