A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047873



Internal ID18790404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125207472..125218428hg38UCSC Ensembl
Innerchr11:125077368..125088324hg19UCSC Ensembl
Innerchr11:124582578..124593534hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3810957
hg1910957
hg1810957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1292n100
Supporting Variantsnssv3514404
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047873
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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