A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033198



Internal ID19122420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53047614..53080343hg38UCSC Ensembl
Innerchr8:53960174..53992903hg19UCSC Ensembl
Innerchr8:54122727..54155456hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3832730
hg1932730
hg1832730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7224n100
Supporting Variantsnssv3688668, nssv3688669
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)nsv1033198
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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