A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584940



Internal ID16025663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240971610..241040706hg38UCSC Ensembl
Innerchr2:241911027..241980123hg19UCSC Ensembl
Innerchr2:241559700..241628796hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3869097
hg1969097
hg1869097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv934587
Samples
Known GenesSNED1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584940
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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