A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169556



Internal ID21313789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38203266..38340379hg38UCSC Ensembl
Outerchr11:38198170..38348573hg38UCSC Ensembl
Innerchr11:38224816..38361929hg19UCSC Ensembl
Outerchr11:38219720..38370123hg19UCSC Ensembl
Innerchr11:38181392..38318505hg18UCSC Ensembl
Outerchr11:38176296..38326699hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38150404
hg19150404
hg18150404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247629, nssv14252291
SamplesMLY_15, MLY_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169556
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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