A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515422



Internal ID18467017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125205392..125225209hg38UCSC Ensembl
Innerchr11:125075288..125095105hg19UCSC Ensembl
Innerchr11:124580498..124600315hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3819818
hg1919818
hg1819818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045657
Supporting Variants
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)nssv3515422
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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