A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7309



Internal ID15552305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49920410..49971037hg38UCSC Ensembl
Outerchr19:50423667..50474294hg19UCSC Ensembl
Outerchr19:55115479..55166106hg18UCSC Ensembl
Outerchr19:55115479..55166106hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3850628
hg1950628
hg1850628
hg1750628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5752, nssv1462
SamplesNA19240, NA19129
Known GenesATF5, IL4I1, MIR4751, NUP62, SIGLEC11, SIGLEC16
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)nsv7309
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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