A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703890



Internal ID15093856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12299150..12315975hg38UCSC Ensembl
Innerchr11:12320697..12337522hg19UCSC Ensembl
Innerchr11:12277273..12294098hg18UCSC Ensembl
Innerchr11:12277273..12294098hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3816826
hg1916826
hg1816826
hg1716826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527449
Supporting Variants
Samples
Known GenesMICALCL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703890
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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