A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067519



Internal ID18810050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36831101..36941830hg38UCSC Ensembl
Innerchr18:34411064..34521793hg19UCSC Ensembl
Innerchr18:32665062..32775791hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38110730
hg19110730
hg18110730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3334n100
Supporting Variantsnssv3564200
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)nsv1067519
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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