A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612874



Internal ID16400283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143618822..143631836hg38UCSC Ensembl
Innerchr8:144700992..144714006hg19UCSC Ensembl
Innerchr8:144772135..144785149hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3813015
hg1913015
hg1813015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12427n54
Supporting Variantsnssv1125699, nssv1125704, nssv1125706, nssv1125707, nssv1125703, nssv1125701, nssv1125705, nssv1125700, nssv1125702, nssv1125697, nssv1125698
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612874
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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