A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055560



Internal ID19144779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967667..38979290hg38UCSC Ensembl
Innerchr22:39363672..39375295hg19UCSC Ensembl
Innerchr22:37693618..37705241hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3811624
hg1911624
hg1811624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4570n100
Supporting Variantsnssv3590782, nssv3590779, nssv3590783, nssv3590784, nssv3737347, nssv3737345, nssv3737340, nssv3737346, nssv3590766, nssv3590765, nssv3590776, nssv3590755, nssv3737344, nssv3590768, nssv3590770, nssv3737342, nssv3590754, nssv3590780, nssv3590761, nssv3590781, nssv3590775, nssv3590769, nssv3737343, nssv3590777, nssv3590753, nssv3590758, nssv3590773, nssv3590759, nssv3590756, nssv3590760, nssv3737341, nssv3590763, nssv3590774, nssv3590764, nssv3590762, nssv3737339, nssv3590771, nssv3737348, nssv3590767, nssv3590757, nssv3590772, nssv3590778
Samples
Known GenesAPOBEC3A_B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055560
Frequency
Sample Size11257
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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