A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021406



Internal ID19110623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12408562..12616131hg38UCSC Ensembl
Innerchr8:12266071..12473640hg19UCSC Ensembl
Innerchr8:12310442..12518011hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38207570
hg19207570
hg18207570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7056n100
Supporting Variantsnssv3666902
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)nsv1021406
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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