A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562160



Internal ID16349569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68666813..68694071hg38UCSC Ensembl
Innerchr13:69240945..69268203hg19UCSC Ensembl
Innerchr13:68138946..68166204hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3827259
hg1927259
hg1827259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3226n54
Supporting Variantsnssv813448, nssv813449
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562160
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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