A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10035



Internal ID15542762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:105741843..105883987hg38UCSC Ensembl
Outerchr14:106208180..106349845hg19UCSC Ensembl
Outerchr14:105279225..105420890hg18UCSC Ensembl
Outerchr14:105279225..105420890hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38142145
hg19141666
hg18141666
hg17141666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
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)nssv10035
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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