A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551484



Internal ID15992207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70689573..70690176hg38UCSC Ensembl
Innerchr10:72449329..72449932hg19UCSC Ensembl
Innerchr10:72119335..72119938hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38604
hg19604
hg18604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1257n54
Supporting Variantsnssv750241
Samples
Known GenesADAMTS14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551484
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