A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695222



Internal ID15431874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1610950..1620419hg38UCSC Ensembl
Innerchr11:1632180..1641649hg19UCSC Ensembl
Innerchr11:1588756..1598225hg18UCSC Ensembl
Innerchr11:1588756..1598225hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg389470
hg199470
hg189470
hg179470
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517817
Supporting Variants
Samples
Known GenesMOB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695222
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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