A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000774



Internal ID16947040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:23561314..23579113hg38UCSC Ensembl
Outerchr22:23903501..23921300hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3817800
hg1917800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953052
Supporting Variants
SamplesBILGI_BIOE
Known GenesIGLL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000774
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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