A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829871



Internal ID6155595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:53666543..53848720hg19UCSC Ensembl
Outerchr1:53439131..53621308hg18UCSC Ensembl
Outerchr1:53378564..53560741hg17UCSC Ensembl
Cytoband1p32.3
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 Variantsnssv1446595
Samples
Known GenesC1orf123, CPT2, LOC100507564, LRP8, MAGOH
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv829871
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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