A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7000n100



Internal ID22793087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8114804..8291288hg38UCSC Ensembl
chr8:7972326..8148810hg19UCSC Ensembl
chr8:8009736..8186220hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38176485
hg19176485
hg18176485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016780, nsv1017746, nsv1022641, nsv1026278, nsv1023546, nsv1026631, nsv1025044, nsv1016286
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7000n100
Frequency
Sample Size11257
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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