A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517486



Internal ID18815767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92091068..92113014hg38UCSC Ensembl
Innerchr11:91824234..91846180hg19UCSC Ensembl
Innerchr11:91463882..91485828hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3821947
hg1921947
hg1821947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050941
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)nssv3517486
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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