A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517090



Internal ID15444383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66160302..66167718hg38UCSC Ensembl
Innerchr11:65927773..65935189hg19UCSC Ensembl
Innerchr11:65684349..65691765hg18UCSC Ensembl
Innerchr11:65684349..65691765hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387417
hg197417
hg187417
hg177417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673779, nssv680503, nssv674079, nssv661871, nssv679870, nssv662191, nssv684902, nssv687441, nssv683045, nssv669371, nssv666891, nssv661270, nssv684043, nssv666549, nssv676316, nssv689744, nssv693092, nssv653851, nssv656388, nssv653770
Samples
Known GenesPACS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517090
Frequency
Sample Size2026
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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