A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029785



Internal ID18772316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18927673..18986188hg38UCSC Ensembl
Innerchr8:18785183..18843698hg19UCSC Ensembl
Innerchr8:18829463..18887978hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3858516
hg1958516
hg1858516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3684197, nssv3684198
Samples
Known GenesPSD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029785
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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