A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519368



Internal ID18470963
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 StatusS
Merged Variantsnsv1050077
Supporting Variants
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)nssv3519368
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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