A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059678



Internal ID18802209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:6155115..6838291hg38UCSC Ensembl
Innerchr18:6155114..6838290hg19UCSC Ensembl
Innerchr18:6145114..6828290hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38683177
hg19683177
hg18683177
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564084
Samples
Known GenesARHGAP28, C18orf64, L3MBTL4, MIR4317
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059678
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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