A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038188



Internal ID18780719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:32388759..32428253hg38UCSC Ensembl
Innerchr11:32410305..32449799hg19UCSC Ensembl
Innerchr11:32366881..32406375hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3839495
hg1939495
hg1839495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508317
Samples
Known GenesWT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038188
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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