A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv946692



Internal ID16240648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:34515061..34543424hg38UCSC Ensembl
Innerchr21:35887359..35915722hg19UCSC Ensembl
Innerchr21:34809229..34837592hg18UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg3828364
hg1928364
hg1828364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587428
Supporting Variants
Samples
Known GenesRCAN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv946692
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