A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021397



Internal ID19110614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12562661hg38UCSC Ensembl
Innerchr8:12260915..12420170hg19UCSC Ensembl
Innerchr8:12305286..12464541hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38159256
hg19159256
hg18159256
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7070n100
Supporting Variantsnssv3665971, nssv3665972
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)nsv1021397
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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