A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581648



Internal ID16022371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:43222999..43227728hg38UCSC Ensembl
Innerchr2:43450138..43454867hg19UCSC Ensembl
Innerchr2:43303642..43308371hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg384730
hg194730
hg184730
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907885
Samples
Known GenesLINC01126, ZFP36L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581648
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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