A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169868



Internal ID21313679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93964770..93972107hg38UCSC Ensembl
Outerchr11:93959164..93974097hg38UCSC Ensembl
Innerchr11:93697936..93705273hg19UCSC Ensembl
Outerchr11:93692330..93707263hg19UCSC Ensembl
Innerchr11:93337584..93344921hg18UCSC Ensembl
Outerchr11:93331978..93346911hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3814934
hg1914934
hg1814934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247122, nssv14249892, nssv14246473, nssv14241404, nssv14244340, nssv14251432, nssv14243238, nssv14252304, nssv14242746, nssv14241601, nssv14241236, nssv14251201, nssv14249214, nssv14249454
SamplesMLY_15, SNI_17, SNI_2, NGO_37, NGO_28, SNI_10, SNI_7, NGO_9, SNI_1, SNI_12, SNI_3, SNI_5, NGO_5, SNI_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169868
Frequency
Sample Size93
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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