A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015987



Internal ID19105205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12406228..12585534hg38UCSC Ensembl
Innerchr8:12263737..12443043hg19UCSC Ensembl
Innerchr8:12308108..12487414hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38179307
hg19179307
hg18179307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7054n100
Supporting Variantsnssv3666892, nssv3760178, nssv3666895, nssv3666893, nssv3666894
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015987
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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