A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833854



Internal ID6159578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:48753400..48927424hg19UCSC Ensembl
Outerchr19:53445212..53619236hg18UCSC Ensembl
Outerchr19:53445212..53619236hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1454766, nssv1454768, nssv1454767
Samples
Known GenesCARD8, CCDC114, EMP3, GRIN2D, KDELR1, LOC100505812, SYNGR4, TMEM143, ZNF114
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833854
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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