A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581647



Internal ID16022370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43222999..43227061hg38UCSC Ensembl
Innerchr2:43450138..43454200hg19UCSC Ensembl
Innerchr2:43303642..43307704hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg384063
hg194063
hg184063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907884
Samples
Known GenesZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581647
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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