A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563360



Internal ID16004083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113398155..113399828hg38UCSC Ensembl
Innerchr13:114052470..114054143hg19UCSC Ensembl
Innerchr13:113100471..113102144hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381674
hg191674
hg181674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3447n54
Supporting Variantsnssv820629
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563360
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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