A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056380



Internal ID19145599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38950674..38979290hg38UCSC Ensembl
Innerchr22:39346679..39375295hg19UCSC Ensembl
Innerchr22:37676625..37705241hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3828617
hg1928617
hg1828617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4568n100
Supporting Variantsnssv3600890, nssv3600889, nssv3600891
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)nsv1056380
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer