A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036096



Internal ID18778627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4234887..4367675hg38UCSC Ensembl
Innerchr11:4256117..4388905hg19UCSC Ensembl
Innerchr11:4212693..4345481hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38132789
hg19132789
hg18132789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1023n100
Supporting Variantsnssv3503344
Samples
Known GenesOR52B4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036096
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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