A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029401



Internal ID19118620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78454025..78515252hg38UCSC Ensembl
Innerchr8:79366260..79427487hg19UCSC Ensembl
Innerchr8:79528815..79590042hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3861228
hg1961228
hg1861228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689581
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)nsv1029401
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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