A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832864



Internal ID6158588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:94828438..95004487hg19UCSC Ensembl
Outerchr14:93898191..94074240hg18UCSC Ensembl
Outerchr14:93898191..94074240hg17UCSC Ensembl
Cytoband14q32.13
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 Variantsnssv1451137, nssv1451138
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)nsv832864
Frequency
Sample Size95
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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