A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7180n100



Internal ID22793267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39426673..39539496hg38UCSC Ensembl
chr8:39284192..39397015hg19UCSC Ensembl
chr8:39403349..39516172hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38112824
hg19112824
hg18112824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019380, nsv1027344, nsv1027061, nsv1023401, nsv1022380, nsv1019739, nsv1023207, nsv1029249, nsv1028189, nsv1021939, nsv1022332, nsv1028002
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)dgv7180n100
Frequency
Sample Size11257
Observed Gain20
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer