A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090162



Internal ID21269960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11806955..11855024hg38UCSC Ensembl
Innerchr10:11848954..11897023hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3848070
hg1948070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111659
Supporting Variants
Samplessample145
Known GenesPROSER2, PROSER2-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090162
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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