A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832762



Internal ID6158486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:31238634..31414038hg19UCSC Ensembl
Outerchr14:30308385..30483789hg18UCSC Ensembl
Outerchr14:30308385..30483789hg17UCSC Ensembl
Cytoband14q12
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 Variantsnssv1450913
Samples
Known GenesCOCH, LOC100506071, STRN3
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832762
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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