A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550285



Internal ID15991008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28273718..28282931hg38UCSC Ensembl
Innerchr10:28562647..28571860hg19UCSC Ensembl
Innerchr10:28602653..28611866hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg389214
hg199214
hg189214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173876
SamplesHGDP01028
Known GenesMPP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550285
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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