A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829940



Internal ID6155664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:57072341..57262730hg19UCSC Ensembl
Outerchr4:56767098..56957487hg18UCSC Ensembl
Outerchr4:56913269..57103658hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1443669
Samples
Known GenesAASDH, KIAA1211, PPAT
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv829940
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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