A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247899



Internal ID21306221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4247390..4315299hg38UCSC Ensembl
Outerchr11:4241343..4325579hg38UCSC Ensembl
Innerchr11:4268620..4336529hg19UCSC Ensembl
Outerchr11:4262573..4346809hg19UCSC Ensembl
Innerchr11:4225196..4293105hg18UCSC Ensembl
Outerchr11:4219149..4303385hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3884237
hg1984237
hg1884237
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesNGO_26
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247899
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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