A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011480



Internal ID19100697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153662179..153696205hg38UCSC Ensembl
Innerchr3:153379968..153413994hg19UCSC Ensembl
Innerchr3:154862658..154896684hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3834027
hg1934027
hg1834027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741544
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)nsv1011480
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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