A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126013



Internal ID18908404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:25259889..25585613hg38UCSC Ensembl
Outerchr22:25655856..25981580hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38325725
hg19325725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984221
SamplesKWS1
Known GenesADRBK2, CRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126013
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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