A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10038



Internal ID15542759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:106294536..106360794hg38UCSC Ensembl
Outerchr14:106751131..106816723hg19UCSC Ensembl
Outerchr14:105822176..105887768hg18UCSC Ensembl
Outerchr14:105822176..105887768hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3866259
hg1965593
hg1865593
hg1765593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1443
Supporting Variants
SamplesNA18956
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)nssv10038
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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