A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015363



Internal ID19104580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88695038..89145861hg38UCSC Ensembl
Innerchr8:89707267..90158090hg19UCSC Ensembl
Innerchr8:89776383..90227206hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38450824
hg19450824
hg18450824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7265n100
Supporting Variantsnssv3689691
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)nsv1015363
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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