A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9226



Internal ID15534638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:85668462..85702253hg38UCSC Ensembl
Outerchr14:86134806..86168597hg19UCSC Ensembl
Outerchr14:85204559..85238350hg18UCSC Ensembl
Outerchr14:85204559..85238350hg17UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg385648
hg195648
hg185648
hg175648
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1385
Supporting Variants
SamplesNA12156
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)nssv9226
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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