A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249292



Internal ID21310236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81588423..81811590hg38UCSC Ensembl
Outerchr11:81587570..81812939hg38UCSC Ensembl
Innerchr11:81299465..81522632hg19UCSC Ensembl
Outerchr11:81298612..81523981hg19UCSC Ensembl
Innerchr11:80977113..81200280hg18UCSC Ensembl
Outerchr11:80976260..81201629hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38225370
hg19225370
hg18225370
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169699
Supporting Variants
SamplesNGO_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249292
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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