A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833850



Internal ID6159574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:47206542..47370310hg19UCSC Ensembl
Outerchr19:51898382..52062150hg18UCSC Ensembl
Outerchr19:51898382..52062150hg17UCSC 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 Variantsnssv1454758, nssv1454757, nssv1454756
Samples
Known GenesAP2S1, FKRP, MIR320E, PRKD2, SLC1A5, SNAR-E, STRN4
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833850
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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