A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036435



Internal ID19125654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:91199863..91316190hg38UCSC Ensembl
Innerchr11:90933031..91049357hg19UCSC Ensembl
Innerchr11:90572679..90689005hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38116328
hg19116327
hg18116327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502942
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)nsv1036435
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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