A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7251



Internal ID15205556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:34502488..34589582hg38UCSC Ensembl
Outerchr14:34971694..35058788hg19UCSC Ensembl
Outerchr14:34041445..34128539hg18UCSC Ensembl
Outerchr14:34041445..34128539hg17UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3887095
hg1987095
hg1887095
hg1787095
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5496, nssv10918, nssv10917
SamplesNA15510, NA19129
Known GenesEAPP, SNX6
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)nsv7251
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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