A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040043



Internal ID18782574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28096904..28149137hg38UCSC Ensembl
Innerchr11:28118451..28170684hg19UCSC Ensembl
Innerchr11:28075027..28127260hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3852234
hg1952234
hg1852234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710073, nssv3710074
Samples
Known GenesKIF18A, METTL15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040043
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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