A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1462



Internal ID15544243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:49920410..49970809hg38UCSC Ensembl
Outerchr19:50423667..50474066hg19UCSC Ensembl
Outerchr19:55115479..55165878hg18UCSC Ensembl
Outerchr19:55115479..55165878hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3850400
hg1950400
hg1850400
hg1750400
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7309
Supporting Variants
SamplesNA19240
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)nssv1462
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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