A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011428



Internal ID19100645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:49612556..49668635hg38UCSC Ensembl
Innerchr3:49649989..49706068hg19UCSC Ensembl
Innerchr3:49624993..49681072hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3856080
hg1956080
hg1856080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3595254
Samples
Known GenesBSN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011428
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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