A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11118



Internal ID15192775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179645886..179689316hg38UCSC Ensembl
Outerchr5:179072887..179116317hg19UCSC Ensembl
Outerchr5:179005493..179048923hg18UCSC Ensembl
Outerchr5:179005493..179048923hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3843431
hg1943431
hg1843431
hg1743431
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7375
Supporting Variants
SamplesNA15510
Known GenesCBY3
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)nssv11118
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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