A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590367



Internal ID16377776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57471713..57508411hg38UCSC Ensembl
Innerchr3:57457440..57494138hg19UCSC Ensembl
Innerchr3:57432480..57469178hg18UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3836699
hg1936699
hg1836699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963366
Samples
Known GenesDNAH12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590367
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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