A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830652



Internal ID6156376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:45187467..45328983hg19UCSC Ensembl
Outerchr6:45295445..45436961hg18UCSC Ensembl
Outerchr6:45295445..45436961hg17UCSC Ensembl
Cytoband6p12.3
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 Variantsnssv1445392
Samples
Known GenesRUNX2, SUPT3H
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv830652
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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