A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022390



Internal ID19111608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8101428..8234503hg38UCSC Ensembl
Innerchr8:7958950..8092025hg19UCSC Ensembl
Innerchr8:7996360..8129435hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38133076
hg19133076
hg18133076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6995n100
Supporting Variantsnssv3681619
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)nsv1022390
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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