A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032150



Internal ID19121372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12376730..12555281hg38UCSC Ensembl
Innerchr8:12234239..12412790hg19UCSC Ensembl
Innerchr8:12278610..12457161hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38178552
hg19178552
hg18178552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7053n100
Supporting Variantsnssv3663762
Samples
Known GenesDEFB109P1, FAM66A, FAM86B2, FAM90A25P, 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)nsv1032150
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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