A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518274



Internal ID18469869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5161946..5240240hg38UCSC Ensembl
Innerchr11:5183176..5261470hg19UCSC Ensembl
Innerchr11:5139752..5218046hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3878295
hg1978295
hg1878295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048593
Supporting Variants
Samples
Known GenesHBB, 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)nssv3518274
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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