A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125798



Internal ID15632298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:144435160..144450108hg38UCSC Ensembl
Innerchr8:145660543..145675491hg19UCSC Ensembl
Innerchr8:145631351..145646299hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3814949
hg1914949
hg1814949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612938
Supporting Variants
Samples
Known GenesCYHR1, LOC100287098, MIR6893, TONSL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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