A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612062



Internal ID16399471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119122886..119148901hg38UCSC Ensembl
Innerchr8:120135125..120161140hg19UCSC Ensembl
Innerchr8:120204306..120230321hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3826016
hg1926016
hg1826016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1120148
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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