A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3334n100



Internal ID20154950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36831101..36959363hg38UCSC Ensembl
chr18:34411064..34539326hg19UCSC Ensembl
chr18:32665062..32793324hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38128263
hg19128263
hg18128263
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064385, nsv1067519
Samples
Known GenesKIAA1328
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3334n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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