A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088743



Internal ID21280390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21170839..21177163hg38UCSC Ensembl
Innerchr10:21459768..21466092hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg386325
hg196325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111412
Supporting Variants
Samplessample296
Known GenesNEBL, NEBL-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088743
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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