A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953055



Internal ID16955242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:23957314..23992806hg38UCSC Ensembl
Outerchr22:24299501..24335000hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3835493
hg1935500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000777
SamplesBILGI_BIOE
Known GenesDDT, DDTL, GSTT2, GSTT2B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953055
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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