A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7037n100



Internal ID22793124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12331722..12616361hg38UCSC Ensembl
chr8:12189231..12473870hg19UCSC Ensembl
chr8:12233602..12518241hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38284640
hg19284640
hg18284640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020506, nsv1034201
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)dgv7037n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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