A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3507921



Internal ID18806202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116101490..116125970hg38UCSC Ensembl
Innerchr11:115972207..115996687hg19UCSC Ensembl
Innerchr11:115477417..115501897hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3824481
hg1924481
hg1824481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045102
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)nssv3507921
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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