A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584154



Internal ID16371563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:196927842..197059077hg38UCSC Ensembl
Innerchr2:197792566..197923801hg19UCSC Ensembl
Innerchr2:197500811..197632046hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38131236
hg19131236
hg18131236
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv930348
Samples
Known GenesANKRD44
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584154
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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