A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583253



Internal ID16370662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:145978777..146036056hg38UCSC Ensembl
Innerchr2:146736345..146793624hg19UCSC Ensembl
Innerchr2:146452815..146510094hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3857280
hg1957280
hg1857280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7097n54
Supporting Variantsnssv920285
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583253
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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