A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038848



Internal ID18781379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125205543..125221672hg38UCSC Ensembl
Innerchr11:125075439..125091568hg19UCSC Ensembl
Innerchr11:124580649..124596778hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3816130
hg1916130
hg1816130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1293n100
Supporting Variantsnssv3506806
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)nsv1038848
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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