A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515828



Internal ID15096435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113162184..113194571hg38UCSC Ensembl
Innerchr11:113032906..113065293hg19UCSC Ensembl
Innerchr11:112538116..112570503hg18UCSC Ensembl
Innerchr11:112538116..112570503hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3832388
hg1932388
hg1832388
hg1732388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664912, nssv688254
Samples
Known GenesNCAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515828
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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