A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1426



Internal ID15199303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:101001693..101033511hg38UCSC Ensembl
Outerchr14:101468030..101499848hg19UCSC Ensembl
Outerchr14:100537783..100569601hg18UCSC Ensembl
Outerchr14:100537783..100569601hg17UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385769
hg195769
hg185769
hg175769
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4131
SamplesNA12878
Known GenesMIR1193, MIR1197, MIR299, MIR323A, MIR329-1, MIR329-2, MIR379, MIR380, MIR411, MIR494, MIR543, MIR758
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)nsv1426
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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