A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508239



Internal ID18806520
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 StatusS
Merged Variantsnsv1052079
Supporting Variants
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)nssv3508239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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