A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611096



Internal ID16398505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40324113..40332030hg38UCSC Ensembl
Innerchr8:40181632..40189549hg19UCSC Ensembl
Innerchr8:40300789..40308706hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg387918
hg197918
hg187918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12114n54
Supporting Variantsnssv1111267, nssv1111268, nssv1111269
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611096
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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