A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611354



Internal ID16398763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:52015829..52035617hg38UCSC Ensembl
Innerchr8:52928389..52948177hg19UCSC Ensembl
Innerchr8:53090942..53110730hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3819789
hg1919789
hg1819789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115323
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611354
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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