A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950587



Internal ID17299461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:185520347..185522946hg38UCSC Ensembl
Outerchr4:186441501..186444100hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv159n73
Supporting Variantsnssv2996823
SamplesBILGI_BIOE
Known GenesPDLIM3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950587
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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