A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592448



Internal ID16033171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164935636..165075970hg38UCSC Ensembl
Innerchr3:164653424..164793758hg19UCSC Ensembl
Innerchr3:166136118..166276452hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38140335
hg19140335
hg18140335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8717n54
Supporting Variantsnssv981121, nssv981122
Samples
Known GenesSI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592448
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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