A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042465



Internal ID18784996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125199208..125213796hg38UCSC Ensembl
Innerchr11:125069104..125083692hg19UCSC Ensembl
Innerchr11:124574314..124588902hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3814589
hg1914589
hg1814589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1291n100
Supporting Variantsnssv3506753
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)nsv1042465
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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