A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516879



Internal ID15444172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25100812..25271637hg38UCSC Ensembl
Innerchr11:25122358..25293183hg19UCSC Ensembl
Innerchr11:25078934..25249759hg18UCSC Ensembl
Innerchr11:25078934..25249759hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38170826
hg19170826
hg18170826
hg17170826
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656563, nssv660706, nssv661939, nssv658870, nssv675330, nssv675720, nssv654638, nssv662809
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516879
Frequency
Sample Size2026
Observed Gain2
Observed Loss6
Observed Complex0
Frequencyn/a


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