A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512571



Internal ID18810852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3428196..3591901hg38UCSC Ensembl
Innerchr11:3449426..3613131hg19UCSC Ensembl
Innerchr11:3406002..3569707hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38163706
hg19163706
hg18163706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042782
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512571
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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