A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022120



Internal ID18764654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12176786..12649550hg38UCSC Ensembl
Innerchr8:12034295..12507059hg19UCSC Ensembl
Innerchr8:12071704..12551430hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38472765
hg19472765
hg18479727
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7019n100
Supporting Variantsnssv3754350, nssv3754352, nssv3754351
Samples
Known GenesDEFB109P1, DEFB130, FAM66A, FAM86B1, FAM86B2, FAM90A25P, FAM90A2P, LOC100133267, LOC100506990, LOC649352, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022120
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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