A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032822



Internal ID19122044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8078321..8237241hg38UCSC Ensembl
Innerchr8:7935843..8094763hg19UCSC Ensembl
Innerchr8:7973253..8132173hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38158921
hg19158921
hg18158921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6996n100
Supporting Variantsnssv3681578
Samples
Known GenesFAM86B3P, MIR548I3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032822
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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