A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv398



Internal ID15198404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87933767..87970853hg38UCSC Ensembl
Outerchr4:88854919..88892005hg19UCSC Ensembl
Outerchr4:89073943..89111029hg18UCSC Ensembl
Outerchr4:89212098..89249184hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3837087
hg1937087
hg1837087
hg1737087
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA19240
Known Genes
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)nssv398
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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