A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125562



Internal ID15978748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:143616727..143631764hg38UCSC Ensembl
Innerchr8:144698897..144713934hg19UCSC Ensembl
Innerchr8:144770040..144785077hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3815038
hg1915038
hg1815038
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612854
Supporting Variants
Samples
Known GenesTSTA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125562
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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