A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022276



Internal ID19111494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12389834..12581370hg38UCSC Ensembl
Innerchr8:12247343..12438879hg19UCSC Ensembl
Innerchr8:12291714..12483250hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38191537
hg19191537
hg18191537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7060n100
Supporting Variantsnssv3760101
Samples
Known GenesDEFB109P1, FAM66A, 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)nsv1022276
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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