A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250809



Internal ID21306457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38967614..39003307hg38UCSC Ensembl
Outerchr22:38955461..39007789hg38UCSC Ensembl
Innerchr22:39363619..39399312hg19UCSC Ensembl
Outerchr22:39351466..39403794hg19UCSC Ensembl
Innerchr22:37693565..37729258hg18UCSC Ensembl
Outerchr22:37681412..37733740hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3852329
hg1952329
hg1852329
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170058
Supporting Variants
SamplesNGO_28
Known GenesAPOBEC3A, APOBEC3A_B, APOBEC3B, APOBEC3B-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250809
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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