A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765564



Internal ID19315078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26901536..26903737hg38UCSC Ensembl
chr22:27297499..27299700hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072632
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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