A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024428



Internal ID19113645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12500660hg38UCSC Ensembl
Innerchr8:12260915..12358169hg19UCSC Ensembl
Innerchr8:12305286..12402540hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3897255
hg1997255
hg1897255
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7068n100
Supporting Variantsnssv3760123, nssv3665835, nssv3760124
Samples
Known GenesFAM66A, 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)nsv1024428
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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