A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833743



Internal ID6159467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10188325..10362589hg19UCSC Ensembl
Outerchr19:10049325..10223589hg18UCSC Ensembl
Outerchr19:10049325..10223589hg17UCSC Ensembl
Cytoband19p13.2
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 Variantsnssv1454530, nssv1454528, nssv1454529
Samples
Known GenesANGPTL6, C19orf66, DNMT1, EIF3G, MIR4322, P2RY11, PPAN, PPAN-P2RY11, S1PR2, SNORD105, SNORD105B
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv833743
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer