A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047571



Internal ID15900757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:284613..381918hg38UCSC Ensembl
Innerchr6:284613..381918hg19UCSC Ensembl
Innerchr6:229613..326918hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3897306
hg1997306
hg1897306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600763
Supporting Variants
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047571
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