A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000798



Internal ID17293750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:35341808..35345507hg38UCSC Ensembl
Outerchr22:35737801..35741500hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953076
Supporting Variants
SamplesBILGI_BIOE
Known GenesTOM1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000798
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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