A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5496



Internal ID15543971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:34509465..34554329hg38UCSC Ensembl
Outerchr14:34978671..35023535hg19UCSC Ensembl
Outerchr14:34048422..34093286hg18UCSC Ensembl
Outerchr14:34048422..34093286hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3844865
hg1944865
hg1844865
hg1744865
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7251
Supporting Variants
SamplesNA19129
Known GenesEAPP
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)nssv5496
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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