A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562200



Internal ID16349609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68938680..69009515hg38UCSC Ensembl
Innerchr13:69512812..69583647hg19UCSC Ensembl
Innerchr13:68410813..68481648hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3870836
hg1970836
hg1870836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813687
Samples
Known GenesMIR548H4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562200
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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