A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583169



Internal ID16023892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:134101185..134135876hg38UCSC Ensembl
Innerchr2:134858756..134893447hg19UCSC Ensembl
Innerchr2:134575226..134609917hg18UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3834692
hg1934692
hg1834692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7088n54
Supporting Variantsnssv920094
Samples
Known GenesMIR3679
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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