A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051904



Internal ID18794435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3881996..3917956hg38UCSC Ensembl
Innerchr11:3903226..3939186hg19UCSC Ensembl
Innerchr11:3859802..3895762hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3835961
hg1935961
hg1835961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1019n100
Supporting Variantsnssv3521857
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)nsv1051904
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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