A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169699



Internal ID21313510
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249292, nssv14243264
SamplesNGO_4, NGO_6
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169699
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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