A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9213



Internal ID15534651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:69271966..69305618hg38UCSC Ensembl
Outerchr14:69738683..69772335hg19UCSC Ensembl
Outerchr14:68808436..68842088hg18UCSC Ensembl
Outerchr14:68808436..68842088hg17UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg385784
hg195784
hg185784
hg175784
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1333
Supporting Variants
SamplesNA12156
Known GenesGALNT16
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)nssv9213
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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