A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581649



Internal ID16022372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43224732..43226264hg38UCSC Ensembl
Innerchr2:43451871..43453403hg19UCSC Ensembl
Innerchr2:43305375..43306907hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381533
hg191533
hg181533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907886
Samples
Known GenesZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581649
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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