A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562695



Internal ID16350104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91339903..91349218hg38UCSC Ensembl
Innerchr13:91992157..92001472hg19UCSC Ensembl
Innerchr13:90790158..90799473hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg389316
hg199316
hg189316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3313n54
Supporting Variantsnssv817416
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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