A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679892



Internal ID15416544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95953622..95968431hg38UCSC Ensembl
Innerchr11:95686786..95701595hg19UCSC Ensembl
Innerchr11:95326434..95341243hg18UCSC Ensembl
Innerchr11:95326434..95341243hg17UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3814810
hg1914810
hg1814810
hg1714810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517358
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679892
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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