A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513303



Internal ID18811584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:109215095..109411802hg38UCSC Ensembl
Innerchr11:109085822..109282528hg19UCSC Ensembl
Innerchr11:108591032..108787738hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38196708
hg19196707
hg18196707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041669
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513303
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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