A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169676



Internal ID21313487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:42948034..42949618hg38UCSC Ensembl
Outerchr11:42940281..42955081hg38UCSC Ensembl
Innerchr11:42969584..42971168hg19UCSC Ensembl
Outerchr11:42961831..42976631hg19UCSC Ensembl
Innerchr11:42926160..42927744hg18UCSC Ensembl
Outerchr11:42918407..42933207hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814801
hg1914801
hg1814801
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246558, nssv14247417, nssv14245246, nssv14246953, nssv14242129, nssv14246492, nssv14244081, nssv14242190, nssv14247799, nssv14247863, nssv14252025
SamplesNGO_27, NGO_41, NGO_28, NGO_43, NGO_31, NGO_35, MLY_9, NGO_36, NGO_48, NGO_44, NGO_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169676
Frequency
Sample Size93
Observed Gain10
Observed Loss1
Observed Complex0
Frequencyn/a


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