A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7072n100



Internal ID22793159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12410961..12532643hg38UCSC Ensembl
chr8:12268470..12390152hg19UCSC Ensembl
chr8:12312841..12434523hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38121683
hg19121683
hg18121683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025785, nsv1024072, nsv1026923, nsv1026502
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7072n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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