A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587476



Internal ID16374885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38744120..38785200hg38UCSC Ensembl
Innerchr21:40116044..40157124hg19UCSC Ensembl
Innerchr21:39037914..39078994hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3841081
hg1941081
hg1841081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7833n54
Supporting Variantsnssv1152405
SamplesHGDP00197
Known GenesLINC00114
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587476
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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