A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612707



Internal ID16400116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142487855..142518691hg38UCSC Ensembl
Innerchr8:143569216..143600052hg19UCSC Ensembl
Innerchr8:143566218..143597054hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3830837
hg1930837
hg1830837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1124931
Samples
Known GenesBAI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612707
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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