A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144025



Internal ID19274153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:38997695..38998195hg38UCSC Ensembl
Outerchr22:39393700..39394200hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994739
SamplesKWS1
Known GenesAPOBEC3B-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144025
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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