A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025044



Internal ID19114262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8144839..8288477hg38UCSC Ensembl
Innerchr8:8002361..8145999hg19UCSC Ensembl
Innerchr8:8039771..8183409hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38143639
hg19143639
hg18143639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7000n100
Supporting Variantsnssv3681634, nssv3754215, nssv3754214, nssv3681635, nssv3754213
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)nsv1025044
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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