A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132565



Internal ID19280516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:16367238..16386738hg38UCSC Ensembl
Outerchr22:16847900..16867400hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3819501
hg1919501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2422n106
Supporting Variantsnssv3987348
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132565
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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