A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955529



Internal ID17304402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184159053..184159611hg38UCSC Ensembl
Outerchr3:183876841..183877399hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv131n73
Supporting Variantsnssv3004477
SamplesBILGI_BIOE
Known GenesDVL3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955529
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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