A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831401



Internal ID6157125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:95218297..95393968hg19UCSC Ensembl
Outerchr8:95287473..95463144hg18UCSC Ensembl
Outerchr8:95287473..95463144hg17UCSC Ensembl
Cytoband8q22.1
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 Variantsnssv1447398
Samples
Known GenesCDH17, GEM, RAD54B
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831401
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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