A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050077



Internal ID18792608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3881996..3919496hg38UCSC Ensembl
Innerchr11:3903226..3940726hg19UCSC Ensembl
Innerchr11:3859802..3897302hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3837501
hg1937501
hg1837501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1019n100
Supporting Variantsnssv3519368
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)nsv1050077
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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