A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059714



Internal ID19148933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967602..38993734hg38UCSC Ensembl
Innerchr22:39363607..39389739hg19UCSC Ensembl
Innerchr22:37693553..37719685hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3826133
hg1926133
hg1826133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4571n100
Supporting Variantsnssv3590735, nssv3590742, nssv3590743, nssv3590737, nssv3590736, nssv3737336, nssv3590738, nssv3590740, nssv3590739, nssv3590741
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)nsv1059714
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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