A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037020



Internal ID18779551
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 StatusM
Merged Variants
Supporting Variantsnssv3504609
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)nsv1037020
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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