A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550146



Internal ID16337555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20168460..20207341hg38UCSC Ensembl
Innerchr10:20457389..20496270hg19UCSC Ensembl
Innerchr10:20497395..20536276hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3838882
hg1938882
hg1838882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv989n54
Supporting Variantsnssv1174147
SamplesHGDP00671
Known GenesPLXDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550146
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