A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152407



Internal ID15534308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:41458763..41494180hg38UCSC Ensembl
Innerchr21:42830690..42866107hg19UCSC Ensembl
Innerchr21:41752560..41787977hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3835418
hg1935418
hg1835418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587496
Supporting Variants
SamplesNINDS_57
Known GenesMX1, TMPRSS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152407
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