A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611833



Internal ID16399242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:103944477..104124321hg38UCSC Ensembl
Innerchr8:104956705..105136549hg19UCSC Ensembl
Innerchr8:105025881..105205725hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38179845
hg19179845
hg18179845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156145
SamplesHGDP00580
Known GenesRIMS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611833
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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