A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7181n100



Internal ID22793268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39426730..39531593hg38UCSC Ensembl
chr8:39284249..39389112hg19UCSC Ensembl
chr8:39403406..39508269hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38104864
hg19104864
hg18104864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028854, nsv1029165, nsv1027947, nsv1030413, nsv1027840, nsv1019950, nsv1034650, nsv1032605
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)dgv7181n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss125
Observed Complex0
Frequencyn/a


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