A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612852



Internal ID16400261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143616149..143630578hg38UCSC Ensembl
Innerchr8:144698319..144712748hg19UCSC Ensembl
Innerchr8:144769462..144783891hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3814430
hg1914430
hg1814430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12427n54
Supporting Variantsnssv1125560
Samples
Known GenesTSTA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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