A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037093



Internal ID18779624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4234887..4396971hg38UCSC Ensembl
Innerchr11:4256117..4418201hg19UCSC Ensembl
Innerchr11:4212693..4374777hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38162085
hg19162085
hg18162085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1023n100
Supporting Variantsnssv3508990, nssv3503962
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037093
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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