A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045366



Internal ID19134585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30872741..30898883hg38UCSC Ensembl
Innerchr11:30894288..30920430hg19UCSC Ensembl
Innerchr11:30850864..30877006hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3826143
hg1926143
hg1826143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088n100
Supporting Variantsnssv3508175
Samples
Known GenesDCDC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045366
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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