A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600895



Internal ID18552490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38955461..38978698hg38UCSC Ensembl
Innerchr22:39351466..39374703hg19UCSC Ensembl
Innerchr22:37681412..37704649hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3823238
hg1923238
hg1823238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061040
Supporting Variants
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)nssv3600895
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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