A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833596



Internal ID6159320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:19654994..19819473hg19UCSC Ensembl
Outerchr18:17908992..18073471hg18UCSC Ensembl
Outerchr18:17908992..18073471hg17UCSC Ensembl
Cytoband18q11.2
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 Variantsnssv1453916, nssv1453915
Samples
Known GenesGATA6
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833596
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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