A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023257



Internal ID19112474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25116916..25149172hg38UCSC Ensembl
Innerchr8:24974431..25006687hg19UCSC Ensembl
Innerchr8:25030348..25062604hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3832257
hg1932257
hg1832257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7145n100
Supporting Variantsnssv3685446, nssv3685451, nssv3685448, nssv3685444, nssv3685445, nssv3685443, nssv3685449, nssv3685447, nssv3685450
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023257
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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