A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517878



Internal ID15098485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59673798..59713496hg38UCSC Ensembl
Innerchr11:59441271..59480969hg19UCSC Ensembl
Innerchr11:59197847..59237545hg18UCSC Ensembl
Innerchr11:59197847..59237545hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3839699
hg1939699
hg1839699
hg1739699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695285
Samples
Known GenesOR10V1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517878
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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