A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059917



Internal ID18802448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11543..175067hg38UCSC Ensembl
Innerchr18:11543..175067hg19UCSC Ensembl
Innerchr18:1543..165067hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38163525
hg19163525
hg18163525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3300n100
Supporting Variantsnssv3569020, nssv3569021
Samples
Known GenesMIR8078, ROCK1P1, USP14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059917
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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