A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013352



Internal ID18755883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141822263..142151451hg38UCSC Ensembl
Innerchr3:141541105..141870293hg19UCSC Ensembl
Innerchr3:143023795..143352983hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38329189
hg19329189
hg18329189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606103
Samples
Known GenesATP1B3, TFDP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013352
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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