A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036041



Internal ID19125260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10109471..10190655hg38UCSC Ensembl
Innerchr11:10131018..10212202hg19UCSC Ensembl
Innerchr11:10087594..10168778hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3881185
hg1981185
hg1881185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503288
Samples
Known GenesSBF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036041
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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