A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169612



Internal ID21313423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:36953177..37029948hg38UCSC Ensembl
Outerchr11:36948644..37033281hg38UCSC Ensembl
Innerchr11:36974726..37051498hg19UCSC Ensembl
Outerchr11:36970193..37054831hg19UCSC Ensembl
Innerchr11:36931302..37008074hg18UCSC Ensembl
Outerchr11:36926769..37011407hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3884638
hg1984639
hg1884639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246652
SamplesNGO_52
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169612
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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