A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832863



Internal ID6158587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:94814819..94967824hg19UCSC Ensembl
Outerchr14:93884572..94037577hg18UCSC Ensembl
Outerchr14:93884572..94037577hg17UCSC Ensembl
Cytoband14q32.13
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 Variantsnssv1451136
Samples
Known GenesSERPINA1, SERPINA11, SERPINA12, SERPINA9
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832863
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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