A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710699



Internal ID18662294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89083370..89246678hg38UCSC Ensembl
Innerchr11:88816538..88979846hg19UCSC Ensembl
Innerchr11:88456186..88619494hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38163309
hg19163309
hg18163309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050341
Supporting Variants
Samples
Known GenesTYR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710699
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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