A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018859



Internal ID18761392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:146134466..146217245hg38UCSC Ensembl
Innerchr4:147055618..147138397hg19UCSC Ensembl
Innerchr4:147275068..147357847hg18UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3882780
hg1982780
hg1882780
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636064
Samples
Known GenesLSM6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018859
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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