A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833761



Internal ID6159485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:14109471..14247590hg19UCSC Ensembl
Outerchr19:13970471..14108590hg18UCSC Ensembl
Outerchr19:13970471..14108590hg17UCSC Ensembl
Cytoband19p13.12
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 Variantsnssv1454563, nssv1454562, nssv1454564
Samples
Known GenesASF1B, IL27RA, LOC113230, PALM3, PRKACA, RFX1, RLN3, SAMD1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833761
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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