A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5752



Internal ID15543660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49921857..49971037hg38UCSC Ensembl
Outerchr19:50425114..50474294hg19UCSC Ensembl
Outerchr19:55116926..55166106hg18UCSC Ensembl
Outerchr19:55116926..55166106hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3849181
hg1949181
hg1849181
hg1749181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7309
Supporting Variants
SamplesNA19129
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)nssv5752
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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