A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517550



Internal ID15098157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131775541..131798641hg38UCSC Ensembl
Innerchr11:131645435..131668535hg19UCSC Ensembl
Innerchr11:131150645..131173745hg18UCSC Ensembl
Innerchr11:131150645..131173745hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3823101
hg1923101
hg1823101
hg1723101
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669546, nssv652336, nssv692866, nssv705567, nssv676407, nssv672584, nssv670774, nssv656912, nssv704881
Samples
Known GenesNTM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517550
Frequency
Sample Size2026
Observed Gain7
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer