A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955350



Internal ID16957537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:134574959..134575658hg38UCSC Ensembl
Outerchr3:134293801..134294500hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001467
SamplesBILGI_BIOE
Known GenesCEP63
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955350
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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