A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975802



Internal ID18611009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101638859..101645012hg38UCSC Ensembl
Innerchr10:103398616..103404769hg19UCSC Ensembl
Innerchr10:103388606..103394759hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg386154
hg196154
hg186154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2761357
SamplesHGDP00998
Known GenesFBXW4
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975802
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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