A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831638



Internal ID6157362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:84153059..84322684hg19UCSC Ensembl
Outerchr9:83342879..83512504hg18UCSC Ensembl
Outerchr9:81382613..81552238hg17UCSC Ensembl
Cytoband9q21.31
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 Variantsnssv1447852, nssv1447853
Samples
Known GenesTLE1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831638
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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