A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089805



Internal ID21283750
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 StatusS
Merged Variantsnsv3115770
Supporting Variants
Samplessample349
Known GenesNMT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089805
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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