A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772455



Internal ID19312372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23972110..23991506hg38UCSC Ensembl
chr22:24314299..24333700hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3819397
hg1919402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072629
Supporting Variants
SamplesKWP1
Known GenesDDT, DDTL, GSTT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772455
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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