A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132564



Internal ID19278967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:15348663..15448263hg38UCSC Ensembl
Outerchr22:16529700..16629300hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3899601
hg1999601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2421n106
Supporting Variantsnssv3987347
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132564
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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