A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831780



Internal ID6157504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8075355..8248183hg19UCSC Ensembl
Outerchr10:8115361..8288189hg18UCSC Ensembl
Outerchr10:8115361..8288189hg17UCSC Ensembl
Cytoband10p14
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 Variantsnssv1448189
Samples
Known GenesFLJ45983, GATA3
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831780
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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