A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2089



Internal ID15541372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105707217..106647801hg38UCSC Ensembl
Outerchr14:106173554..107103804hg19UCSC Ensembl
Outerchr14:105244599..106174849hg18UCSC Ensembl
Outerchr14:105244599..106174849hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38940585
hg19930251
hg18930251
hg17930251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA18555
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv2089
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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