A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583918



Internal ID16371327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:182647608..182707769hg38UCSC Ensembl
Innerchr2:183512335..183572496hg19UCSC Ensembl
Innerchr2:183220580..183280741hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3860162
hg1960162
hg1860162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7213n54
Supporting Variantsnssv927861
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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