A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6995n100



Internal ID22793082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8078321..8234503hg38UCSC Ensembl
chr8:7935843..8092025hg19UCSC Ensembl
chr8:7973253..8129435hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38156183
hg19156183
hg18156183
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027909, nsv1028572, nsv1022390
Samples
Known GenesFAM86B3P, MIR548I3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6995n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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