A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517089



Internal ID15444382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105044836..105059949hg38UCSC Ensembl
Innerchr11:104915563..104930676hg19UCSC Ensembl
Innerchr11:104420773..104435886hg18UCSC Ensembl
Innerchr11:104420773..104435886hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3815114
hg1915114
hg1815114
hg1715114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656321, nssv666866, nssv666813, nssv663260, nssv680184, nssv681367, nssv669145, nssv660483, nssv687317, nssv659154, nssv670602, nssv652423, nssv661895, nssv665606, nssv671695, nssv657978, nssv669492, nssv679709, nssv653766, nssv689568, nssv688438, nssv672727, nssv671924, nssv687285, nssv661632, nssv683377, nssv683775, nssv680370, nssv666774, nssv666889, nssv678842, nssv677082, nssv656137, nssv692529, nssv668937, nssv676978, nssv676209, nssv674156, nssv656386, nssv682448, nssv675624, nssv673469, nssv683798, nssv658928
Samples
Known GenesCARD16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517089
Frequency
Sample Size2026
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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