A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029661



Internal ID19118879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:73117142..73135058hg38UCSC Ensembl
Innerchr8:74029377..74047293hg19UCSC Ensembl
Innerchr8:74191931..74209847hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3817917
hg1917917
hg1817917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689558
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)nsv1029661
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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