A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043039



Internal ID18785570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3881996..3933929hg38UCSC Ensembl
Innerchr11:3903226..3955159hg19UCSC Ensembl
Innerchr11:3859802..3911735hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3851934
hg1951934
hg1851934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514735
Samples
Known GenesSTIM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043039
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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