A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122053



Internal ID19282390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:32654914..32694414hg38UCSC Ensembl
Outerchr22:33050900..33090400hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3839501
hg1939501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2454n106
Supporting Variantsnssv3969483
SamplesKWS2
Known GenesSYN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122053
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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