A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010928



Internal ID19100145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4326110..4362842hg38UCSC Ensembl
Innerchr3:4367794..4404526hg19UCSC Ensembl
Innerchr3:4342794..4379526hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3836733
hg1936733
hg1836733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591635
Samples
Known GenesSUMF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010928
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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