A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769323



Internal ID18967681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28883111..28884412hg38UCSC Ensembl
chr22:29279099..29280400hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072633
Supporting Variants
SamplesKWP1
Known GenesZNRF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769323
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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