A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516459



Internal ID15097066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134279180..134346971hg38UCSC Ensembl
Innerchr11:134149074..134216865hg19UCSC Ensembl
Innerchr11:133654284..133722075hg18UCSC Ensembl
Innerchr11:133654284..133722075hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3867792
hg1967792
hg1867792
hg1767792
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684190, nssv683581, nssv703662, nssv692985, nssv691711, nssv672299, nssv683940, nssv668532, nssv677980
Samples
Known GenesGLB1L2, GLB1L3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516459
Frequency
Sample Size2026
Observed Gain3
Observed Loss6
Observed Complex0
Frequencyn/a


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