A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6615



Internal ID15537248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105837089..106347694hg38UCSC Ensembl
Outerchr14:106303423..106803618hg19UCSC Ensembl
Outerchr14:105374468..105874663hg18UCSC Ensembl
Outerchr14:105374468..105874663hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38510606
hg19500196
hg18500196
hg17500196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA12156
Known GenesADAM6, KIAA0125, 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)nssv6615
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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