A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520711



Internal ID18472306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4234887..4365462hg38UCSC Ensembl
Innerchr11:4256117..4386692hg19UCSC Ensembl
Innerchr11:4212693..4343268hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38130576
hg19130576
hg18130576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052915
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)nssv3520711
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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