A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696823



Internal ID15433475
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519381
Supporting Variants
Samples
Known GenesCNTN5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696823
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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