A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552053



Internal ID16339462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:101277891..101311652hg38UCSC Ensembl
Innerchr10:103037648..103071409hg19UCSC Ensembl
Innerchr10:103027638..103061399hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3833762
hg1933762
hg1833762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1374n54
Supporting Variantsnssv756073
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552053
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