A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064230



Internal ID18806761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37421437..37442794hg38UCSC Ensembl
Innerchr18:35001400..35022757hg19UCSC Ensembl
Innerchr18:33255398..33276755hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3821358
hg1921358
hg1821358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564209
Samples
Known GenesCELF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064230
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