A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611119



Internal ID16398528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40373409..40443369hg38UCSC Ensembl
Innerchr8:40230928..40300888hg19UCSC Ensembl
Innerchr8:40350085..40420045hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3869961
hg1969961
hg1869961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1111351
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611119
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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