A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10918



Internal ID15539506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:34553897..34589582hg38UCSC Ensembl
Outerchr14:35023103..35058788hg19UCSC Ensembl
Outerchr14:34092854..34128539hg18UCSC Ensembl
Outerchr14:34092854..34128539hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3835686
hg1935686
hg1835686
hg1735686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7251
Supporting Variants
SamplesNA15510
Known GenesSNX6
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)nssv10918
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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