A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512466



Internal ID18810747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5768359..5787134hg38UCSC Ensembl
Innerchr11:5789589..5808364hg19UCSC Ensembl
Innerchr11:5746165..5764940hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3818776
hg1918776
hg1818776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042175
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)nssv3512466
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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