A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550323



Internal ID15991046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29619199..29651794hg38UCSC Ensembl
Innerchr10:29908128..29940723hg19UCSC Ensembl
Innerchr10:29948134..29980729hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3832596
hg1932596
hg1832596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv745712
Samples
Known GenesSVIL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550323
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