A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014166



Internal ID19103386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162148105..162237872hg38UCSC Ensembl
Innerchr3:161865893..161955660hg19UCSC Ensembl
Innerchr3:163348587..163438354hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3889768
hg1989768
hg1889768
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4932n100
Supporting Variantsnssv3606431, nssv3606435, nssv3606432, nssv3606433, nssv3606434
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)nsv1014166
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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