A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050657



Internal ID19139876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45433881..45462770hg38UCSC Ensembl
Innerchr11:45455431..45484320hg19UCSC Ensembl
Innerchr11:45412007..45440896hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3828890
hg1928890
hg1828890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1110n100
Supporting Variantsnssv3517180
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050657
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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