A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611456



Internal ID16398865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:65847391..65860323hg38UCSC Ensembl
Innerchr8:66759626..66772558hg19UCSC Ensembl
Innerchr8:66922180..66935112hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3812933
hg1912933
hg1812933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115735
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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