A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036414



Internal ID18778945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125202017..125213796hg38UCSC Ensembl
Innerchr11:125071913..125083692hg19UCSC Ensembl
Innerchr11:124577123..124588902hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3811780
hg1911780
hg1811780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1291n100
Supporting Variantsnssv3502923
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)nsv1036414
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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