A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584641



Internal ID16372050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228894612..228895091hg38UCSC Ensembl
Innerchr2:229759328..229759807hg19UCSC Ensembl
Innerchr2:229467572..229468051hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38480
hg19480
hg18480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7328n54
Supporting Variantsnssv933541, nssv933538, nssv933540, nssv933539, nssv933537, nssv933542, nssv933543
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584641
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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