A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3504609



Internal ID18456204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89324258..89393919hg38UCSC Ensembl
Innerchr11:89057426..89127087hg19UCSC Ensembl
Innerchr11:88697074..88766735hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3869662
hg1969662
hg1869662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037020
Supporting Variants
Samples
Known GenesNOX4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3504609
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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