A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563008



Internal ID16350417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105580809..105651875hg38UCSC Ensembl
Innerchr13:106233158..106304224hg19UCSC Ensembl
Innerchr13:105031159..105102225hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3871067
hg1971067
hg1871067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3372n54
Supporting Variantsnssv818886, nssv818877, nssv818863, nssv818869, nssv818867, nssv818860, nssv818875, nssv818880, nssv818862, nssv818865, nssv818878, nssv818874, nssv818864, nssv818876, nssv818884, nssv818861, nssv818870, nssv818879, nssv818858, nssv818881, nssv818859, nssv818872, nssv818871, nssv818885, nssv818882, nssv818866, nssv818883, nssv818868, nssv818873
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563008
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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