A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561704



Internal ID16349113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:54821118..55190498hg38UCSC Ensembl
Innerchr13:55395253..55764633hg19UCSC Ensembl
Innerchr13:54293254..54662634hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38369381
hg19369381
hg18369381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv811793
Samples
Known GenesMIR5007
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561704
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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