A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7178n100



Internal ID22793265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39426673..39511377hg38UCSC Ensembl
chr8:39284192..39368896hg19UCSC Ensembl
chr8:39403349..39488053hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3884705
hg1984705
hg1884705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031956, nsv1031004, nsv1034237, nsv1027002, nsv1025317, nsv1020617, nsv1027911
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7178n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss69
Observed Complex0
Frequencyn/a


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