A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019795



Internal ID19109013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8229622..8283909hg38UCSC Ensembl
Innerchr8:8087144..8141431hg19UCSC Ensembl
Innerchr8:8124554..8178841hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3854288
hg1954288
hg1854288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7002n100
Supporting Variantsnssv3681654
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019795
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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