A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1107302



Internal ID15960488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16604217..16655596hg38UCSC Ensembl
Innerchr8:16461726..16513105hg19UCSC Ensembl
Innerchr8:16506097..16557476hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3851380
hg1951380
hg1851380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610666
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1107302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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