A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003916



Internal ID19093134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145278946..145428482hg38UCSC Ensembl
Innerchr3:144996733..145146269hg19UCSC Ensembl
Innerchr3:146479423..146628959hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38149537
hg19149537
hg18149537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606138
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003916
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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