A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029540



Internal ID19118759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12848366..12941442hg38UCSC Ensembl
Innerchr8:12705875..12798951hg19UCSC Ensembl
Innerchr8:12750246..12843322hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3893077
hg1993077
hg1893077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760195
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029540
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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