A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088565



Internal ID21274109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6635730..6796580hg38UCSC Ensembl
Innerchr10:6677692..6838542hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38160851
hg19160851
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115293
Supporting Variants
Samplessample202
Known GenesLINC00706, LINC00707
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088565
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer