A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9303



Internal ID15540254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105863356..105896910hg38UCSC Ensembl
Outerchr14:106329566..106362768hg19UCSC Ensembl
Outerchr14:105400611..105433813hg18UCSC Ensembl
Outerchr14:105400611..105433813hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3833555
hg1933203
hg1833203
hg1733203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA18517
Known Genes
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)nssv9303
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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