A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694857



Internal ID15431509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39038902..39049549hg38UCSC Ensembl
Innerchr22:39434907..39445554hg19UCSC Ensembl
Innerchr22:37764853..37775500hg18UCSC Ensembl
Innerchr22:37759407..37770054hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3810648
hg1910648
hg1810648
hg1710648
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522083
Supporting Variants
Samples
Known GenesAPOBEC3F
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694857
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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