A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581635



Internal ID16369044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42211468..42235790hg38UCSC Ensembl
Innerchr2:42438608..42462930hg19UCSC Ensembl
Innerchr2:42292112..42316434hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3824323
hg1924323
hg1824323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv907868
Samples
Known GenesEML4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581635
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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