A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710087



Internal ID19008368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37588242..37752532hg38UCSC Ensembl
Innerchr11:37609792..37774082hg19UCSC Ensembl
Innerchr11:37566368..37730658hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38164291
hg19164291
hg18164291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049291
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)nssv3710087
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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