A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953066



Internal ID16955253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:29045113..29052312hg38UCSC Ensembl
Outerchr22:29441101..29448300hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000788
SamplesBILGI_BIOE
Known GenesZNRF3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953066
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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