A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042325



Internal ID19131544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24377551..24411236hg38UCSC Ensembl
Innerchr11:24399097..24432782hg19UCSC Ensembl
Innerchr11:24355673..24389358hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3833686
hg1933686
hg1833686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506597
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)nsv1042325
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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