A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003026



Internal ID18745558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9714810..9872387hg38UCSC Ensembl
Innerchr2:9854939..10012516hg19UCSC Ensembl
Innerchr2:9772390..9929967hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38157578
hg19157578
hg18157578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576951
Samples
Known GenesTAF1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003026
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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