A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517742



Internal ID15445035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134476225..134864402hg38UCSC Ensembl
Innerchr11:134346119..134734296hg19UCSC Ensembl
Innerchr11:133851329..134239506hg18UCSC Ensembl
Innerchr11:133851329..134239506hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38388178
hg19388178
hg18388178
hg17388178
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669370, nssv681851, nssv679070, nssv660554, nssv702829, nssv674297, nssv680301, nssv674825, nssv660646, nssv681246, nssv659587, nssv701282, nssv661185, nssv686858, nssv691551, nssv653074, nssv681096, nssv663316, nssv699881, nssv692642, nssv705029, nssv667462, nssv657982, nssv665328, nssv657093, nssv654353
Samples
Known GenesLOC283177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517742
Frequency
Sample Size2026
Observed Gain20
Observed Loss6
Observed Complex0
Frequencyn/a


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