A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024901



Internal ID19114118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12383056..12505127hg38UCSC Ensembl
Innerchr8:12240565..12362636hg19UCSC Ensembl
Innerchr8:12284936..12407007hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38122072
hg19122072
hg18122072
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7052n100
Supporting Variantsnssv3664874, nssv3664875, nssv3760065, nssv3664873
Samples
Known GenesDEFB109P1, FAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024901
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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