A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065574



Internal ID18808105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38947840..38979290hg38UCSC Ensembl
Innerchr22:39343845..39375295hg19UCSC Ensembl
Innerchr22:37673791..37705241hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3831451
hg1931451
hg1831451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4568n100
Supporting Variantsnssv3734210
Samples
Known GenesAPOBEC3A, APOBEC3A_B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065574
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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