A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060528



Internal ID19149747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967602..38978698hg38UCSC Ensembl
Innerchr22:39363607..39374703hg19UCSC Ensembl
Innerchr22:37693553..37704649hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3811097
hg1911097
hg1811097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4570n100
Supporting Variantsnssv3600913, nssv3600912
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)nsv1060528
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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