A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169496



Internal ID21313979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105788935..105795937hg38UCSC Ensembl
Outerchr4:105782376..105796640hg38UCSC Ensembl
Innerchr4:106710092..106717094hg19UCSC Ensembl
Outerchr4:106703533..106717797hg19UCSC Ensembl
Innerchr4:106929541..106936543hg18UCSC Ensembl
Outerchr4:106922982..106937246hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3814265
hg1914265
hg1814265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241901
SamplesNGO_44
Known GenesGSTCD
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169496
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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