A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060743



Internal ID19149962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967602..38998456hg38UCSC Ensembl
Innerchr22:39363607..39394461hg19UCSC Ensembl
Innerchr22:37693553..37724407hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3830855
hg1930855
hg1830855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4571n100
Supporting Variantsnssv3590744
Samples
Known GenesAPOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060743
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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