A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052079



Internal ID19141298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5762153..5787806hg38UCSC Ensembl
Innerchr11:5783383..5809036hg19UCSC Ensembl
Innerchr11:5739959..5765612hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825654
hg1925654
hg1825654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3516085, nssv3508239
Samples
Known GenesOR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052079
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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