A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569020



Internal ID18520615
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 StatusS
Merged Variantsnsv1059917
Supporting Variants
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)nssv3569020
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