A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833834



Internal ID6159558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:42736444..42835027hg19UCSC Ensembl
Outerchr19:47428284..47526867hg18UCSC Ensembl
Outerchr19:47428284..47526867hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1454730
Samples
Known GenesCIC, ERF, GSK3A, MEGF8, PAFAH1B3, PRR19, TMEM145
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833834
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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