A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037955



Internal ID19127174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89417255..89459141hg38UCSC Ensembl
Innerchr11:89150423..89192309hg19UCSC Ensembl
Innerchr11:88790071..88831957hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3841887
hg1941887
hg1841887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504452
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)nsv1037955
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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