A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519381



Internal ID15446674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:99313871..99330586hg38UCSC Ensembl
Innerchr11:99184602..99201317hg19UCSC Ensembl
Innerchr11:98689812..98706527hg18UCSC Ensembl
Innerchr11:98689812..98706527hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3816716
hg1916716
hg1816716
hg1716716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696823
Samples
Known GenesCNTN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519381
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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