A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169366



Internal ID21313849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12144226..12165294hg38UCSC Ensembl
Outerchr1:12134688..12170574hg38UCSC Ensembl
Innerchr1:12204283..12225351hg19UCSC Ensembl
Outerchr1:12194745..12230631hg19UCSC Ensembl
Innerchr1:12126870..12147938hg18UCSC Ensembl
Outerchr1:12117332..12153218hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3835887
hg1935887
hg1835887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242632
SamplesNGO_25
Known GenesMIR7846, TNFRSF1B, TNFRSF8
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169366
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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