A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111234



Internal ID19248592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:32569295..32569447hg38UCSC Ensembl
Outerchr22:32965281..32965433hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962512
SamplesKWS1
Known GenesSYN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111234
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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