A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770265



Internal ID18966813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19959767..19959940hg38UCSC Ensembl
chr22:19947290..19947463hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071776
Supporting Variants
SamplesKWP1
Known GenesCOMT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770265
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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