A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169511



Internal ID21313744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43545553..43615028hg38UCSC Ensembl
Outerchr11:43544106..43620580hg38UCSC Ensembl
Innerchr11:43567103..43636578hg19UCSC Ensembl
Outerchr11:43565656..43642130hg19UCSC Ensembl
Innerchr11:43523679..43593154hg18UCSC Ensembl
Outerchr11:43522232..43598706hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3876475
hg1976475
hg1876475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245822
SamplesMLY_17
Known GenesMIR129-2, MIR670
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169511
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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