A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017746



Internal ID19106963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8160502..8291288hg38UCSC Ensembl
Innerchr8:8018024..8148810hg19UCSC Ensembl
Innerchr8:8055434..8186220hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38130787
hg19130787
hg18130787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7000n100
Supporting Variantsnssv3681641
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)nsv1017746
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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