A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000803



Internal ID16947069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:39076996..39092195hg38UCSC Ensembl
Outerchr22:39473001..39488200hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3815200
hg1915200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955157
Supporting Variants
SamplesBILGI_BIOE
Known GenesAPOBEC3G
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000803
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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