A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106251



Internal ID15959437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10393248..10436820hg38UCSC Ensembl
Innerchr8:10250758..10294330hg19UCSC Ensembl
Innerchr8:10288168..10331740hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3843573
hg1943573
hg1843573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610266
Supporting Variants
Samples
Known GenesMSRA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106251
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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