A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612861



Internal ID16400270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143616728..143631836hg38UCSC Ensembl
Innerchr8:144698898..144714006hg19UCSC Ensembl
Innerchr8:144770041..144785149hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3815109
hg1915109
hg1815109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12427n54
Supporting Variantsnssv1125571, nssv1125573, nssv1125570, nssv1125572
Samples
Known GenesTSTA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612861
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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