A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515219



Internal ID18466814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5163316..5248100hg38UCSC Ensembl
Innerchr11:5184546..5269330hg19UCSC Ensembl
Innerchr11:5141122..5225906hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3884785
hg1984785
hg1884785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052798
Supporting Variants
Samples
Known GenesHBB, HBBP1, HBD, OR51V1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515219
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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