A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955622



Internal ID17304495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:185520485..185522939hg38UCSC Ensembl
Outerchr4:186441639..186444093hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382455
hg192455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv159n73
Supporting Variantsnssv3000600
SamplesBILGI_BIOE
Known GenesPDLIM3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955622
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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