A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834238



Internal ID6159962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:50841119..50995394hg19UCSC Ensembl
Outerchr22:49187985..49342260hg18UCSC Ensembl
Outerchr22:49131263..49285538hg17UCSC Ensembl
Cytoband22q13.33
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 Variantsnssv1456214, nssv1456215
Samples
Known GenesADM2, C22orf41, KLHDC7B, LMF2, MIOX, NCAPH2, ODF3B, PPP6R2, SBF1, SCO2, TYMP
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv834238
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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